Reference genomeGRCh38hg38
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Read the genes linked to Infertility, and the rest of your genome, with one test.
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Get my Genome Test108 genes linked to Infertility
Changes in these genes cause rare conditions in which Infertility 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 |
|---|---|---|
| APOA1apolipoprotein A1 | Always | In 1 condition |
| CCNOcyclin O | Always | In 1 condition |
| DCAF17DDB1 and CUL4 associated factor 17 | Always | In 1 condition |
| DNAAF1dynein axonemal assembly factor 1 | Always | In 1 condition |
| DNAAF4dynein axonemal assembly factor 4 | Always | In 1 condition |
| DNAH9dynein axonemal heavy chain 9 | Always | In 1 condition |
| FSHBfollicle stimulating hormone subunit beta | Always | In 1 condition |
| RSPH1radial spoke head component 1 | Always | In 1 condition |
| SOX9SRY-box transcription factor 9 | Always | In 1 condition |
| DHHdesert hedgehog signaling molecule | Very often (80–99%) | In 1 condition |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Very often (80–99%) | In 1 condition |
| HSD17B3hydroxysteroid 17-beta dehydrogenase 3 | Very often (80–99%) | In 2 conditions |
| MAGEL2MAGE family member L2 | Very often (80–99%) | In 5 conditions |
| MKRN3makorin ring finger protein 3 | Very often (80–99%) | In 1 condition |
| NPAP1nuclear pore associated protein 1 | Very often (80–99%) | In 1 condition |
| PLIN1perilipin 1 | Very often (80–99%) | In 1 condition |
| PWAR1Prader Willi/Angelman region RNA 1 | Very often (80–99%) | In 1 condition |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Very often (80–99%) | In 1 condition |
| SIM1SIM bHLH transcription factor 1 | Very often (80–99%) | In 1 condition |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Very often (80–99%) | In 1 condition |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Very often (80–99%) | In 1 condition |
| FOXA2forkhead box A2 | Often (30–79%) | In 1 condition |
| GLI2GLI family zinc finger 2 | Often (30–79%) | In 1 condition |
| H6PDhexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase | Often (30–79%) | In 1 condition |
| HESX1HESX homeobox 1 | Often (30–79%) | In 1 condition |
| LHX4LIM homeobox 4 | Often (30–79%) | In 1 condition |
| NDNnecdin, MAGE family member | Often (30–79%) | In 3 conditions |
| OCA2OCA2 melanosomal transmembrane protein | Often (30–79%) | In 3 conditions |
| OTX2orthodenticle homeobox 2 | Often (30–79%) | In 1 condition |
| POU1F1POU class 1 homeobox 1 | Often (30–79%) | In 1 condition |
| PRLRprolactin receptor | Often (30–79%) | In 1 condition |
| PROP1PROP paired-like homeobox 1 | Often (30–79%) | In 2 conditions |
| RSPH3radial spoke head 3 | Often (30–79%) | In 1 condition |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Often (30–79%) | In 3 conditions |
| SOX3SRY-box transcription factor 3 | Often (30–79%) | In 1 condition |
| AIPAHR interacting HSP90 co-chaperone | Sometimes (5–29%) | In 1 condition |
| ANOS1anosmin 1 | Sometimes (5–29%) | In 1 condition |
| ARL6ARF like GTPase 6 | Sometimes (5–29%) | In 1 condition |
| ATP7BATPase copper transporting beta | Sometimes (5–29%) | In 1 condition |
| AXLAXL receptor tyrosine kinase | Sometimes (5–29%) | In 1 condition |
Show 68 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| BBIP1BBSome interacting protein 1 | Sometimes (5–29%) | In 1 condition |
| BBS1Bardet-Biedl syndrome 1 | Sometimes (5–29%) | In 1 condition |
| BBS10Bardet-Biedl syndrome 10 | Sometimes (5–29%) | In 1 condition |
| BBS12Bardet-Biedl syndrome 12 | Sometimes (5–29%) | In 1 condition |
| BBS2Bardet-Biedl syndrome 2 | Sometimes (5–29%) | In 1 condition |
| BBS4Bardet-Biedl syndrome 4 | Sometimes (5–29%) | In 1 condition |
| BBS5Bardet-Biedl syndrome 5 | Sometimes (5–29%) | In 1 condition |
| BBS7Bardet-Biedl syndrome 7 | Sometimes (5–29%) | In 1 condition |
| BBS9Bardet-Biedl syndrome 9 | Sometimes (5–29%) | In 1 condition |
| BMP6bone morphogenetic protein 6 | Sometimes (5–29%) | In 1 condition |
| CCDC141coiled-coil domain containing 141 | Sometimes (5–29%) | In 1 condition |
| CDH23cadherin related 23 | Sometimes (5–29%) | In 1 condition |
| CEP19centrosomal protein 19 | Sometimes (5–29%) | In 2 conditions |
| CEP290centrosomal protein 290 | Sometimes (5–29%) | In 1 condition |
| CFAP418cilia and flagella associated protein 418 | Sometimes (5–29%) | In 1 condition |
| CHD7chromodomain helicase DNA binding protein 7 | Sometimes (5–29%) | In 1 condition |
| DUSP6dual specificity phosphatase 6 | Sometimes (5–29%) | In 1 condition |
| FEZF1FEZ family zinc finger 1 | Sometimes (5–29%) | In 1 condition |
| FGF17fibroblast growth factor 17 | Sometimes (5–29%) | In 1 condition |
| FGF8fibroblast growth factor 8 | Sometimes (5–29%) | In 1 condition |
| FGFR1fibroblast growth factor receptor 1 | Sometimes (5–29%) | In 1 condition |
| FLRT3fibronectin leucine rich transmembrane protein 3 | Sometimes (5–29%) | In 1 condition |
| GBA2glucosylceramidase beta 2 | Sometimes (5–29%) | In 2 conditions |
| GNRH1gonadotropin releasing hormone 1 | Sometimes (5–29%) | In 1 condition |
| GNRHRgonadotropin releasing hormone receptor | Sometimes (5–29%) | In 1 condition |
| GPR101G protein-coupled receptor 101 | Sometimes (5–29%) | In 1 condition |
| HFEhomeostatic iron regulator | Sometimes (5–29%) | In 1 condition |
| HS6ST1heparan sulfate 6-O-sulfotransferase 1 | Sometimes (5–29%) | In 1 condition |
| IFT172intraflagellar transport 172 | Sometimes (5–29%) | In 1 condition |
| IFT27intraflagellar transport 27 | Sometimes (5–29%) | In 1 condition |
| IFT74intraflagellar transport 74 | Sometimes (5–29%) | In 1 condition |
| KISS1KiSS-1 metastasis suppressor | Sometimes (5–29%) | In 1 condition |
| KISS1RKISS1 receptor | Sometimes (5–29%) | In 1 condition |
| LZTFL1leucine zipper transcription factor like 1 | Sometimes (5–29%) | In 1 condition |
| MKKSMKKS centrosomal shuttling protein | Sometimes (5–29%) | In 1 condition |
| MKS1MKS transition zone complex subunit 1 | Sometimes (5–29%) | In 1 condition |
| NPHP1nephrocystin 1 | Sometimes (5–29%) | In 1 condition |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Sometimes (5–29%) | In 2 conditions |
| NSMFNMDA receptor synaptonuclear signaling and neuronal migration factor | Sometimes (5–29%) | In 1 condition |
| PROK2prokineticin 2 | Sometimes (5–29%) | In 1 condition |
| PROKR2prokineticin receptor 2 | Sometimes (5–29%) | In 1 condition |
| SCAPERS-phase cyclin A associated protein in the ER | Sometimes (5–29%) | In 1 condition |
| SCLT1sodium channel and clathrin linker 1 | Sometimes (5–29%) | In 1 condition |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Sometimes (5–29%) | In 1 condition |
| SEMA3Asemaphorin 3A | Sometimes (5–29%) | In 1 condition |
| SEMA3Esemaphorin 3E | Sometimes (5–29%) | In 1 condition |
| SOX10SRY-box transcription factor 10 | Sometimes (5–29%) | In 1 condition |
| SPRY4sprouty RTK signaling antagonist 4 | Sometimes (5–29%) | In 1 condition |
| SRA1steroid receptor RNA activator 1 | Sometimes (5–29%) | In 1 condition |
| TAC3tachykinin precursor 3 | Sometimes (5–29%) | In 1 condition |
| TACR3tachykinin receptor 3 | Sometimes (5–29%) | In 1 condition |
| TRIM32tripartite motif containing 32 | Sometimes (5–29%) | In 1 condition |
| TTC8tetratricopeptide repeat domain 8 | Sometimes (5–29%) | In 1 condition |
| WDPCPWD repeat containing planar cell polarity effector | Sometimes (5–29%) | In 1 condition |
| WDR11WD repeat domain 11 | Sometimes (5–29%) | In 1 condition |
| STUB1STIP1 homology and U-box containing protein 1 | Rarely (1–4%) | In 1 condition |
| ARandrogen receptor | Not recorded | In 1 condition |
| CCDC40coiled-coil domain 40 molecular ruler complex subunit | Not recorded | In 1 condition |
| CFAP298cilia and flagella associated protein 298 | Not recorded | In 1 condition |
| CFAP300cilia and flagella associated protein 300 | Not recorded | In 1 condition |
| DNAAF3dynein axonemal assembly factor 3 | Not recorded | In 1 condition |
| GAS2L2growth arrest specific 2 like 2 | Not recorded | In 1 condition |
| HJVhemojuvelin BMP co-receptor | Not recorded | In 1 condition |
| HLA-DQA1major histocompatibility complex, class II, DQ alpha 1 | Not recorded | In 1 condition |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Not recorded | In 1 condition |
| NANOS1nanos C2HC-type zinc finger 1 | Not recorded | In 1 condition |
| PADI6peptidyl arginine deiminase 6 | 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 2026.10.16-c6eea6bf.
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