Trait
Increased circulating gonadotropin level
Overproduction of gonadotropins (FSH, LH) by the anterior pituitary gland.
Summary
- Also called
- Elevated gonadotropins, Elevated serum gonadotropins, Gonadotropin excess
Reference genomeGRCh38hg38
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Get my Genome Test67 genes linked to Increased circulating gonadotropin level
Changes in these genes cause rare conditions in which Increased circulating gonadotropin level 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 |
|---|---|---|
| BMP15bone morphogenetic protein 15 | Very often (80–99%) | In 1 condition |
| BNC1basonuclin zinc finger protein 1 | Very often (80–99%) | 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 |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Very often (80–99%) | In 1 condition |
| DHHdesert hedgehog signaling molecule | Very often (80–99%) | In 1 condition |
| DHX37DEAH-box helicase 37 | 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 |
| ESR1estrogen receptor 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 1 condition |
| FIGLAfolliculogenesis specific bHLH transcription factor | Very often (80–99%) | In 1 condition |
| FSHRfollicle stimulating hormone receptor | Very often (80–99%) | In 3 conditions |
| GATA4GATA binding protein 4 | Very often (80–99%) | In 1 condition |
| GCNAgerm cell nuclear acidic peptidase | Very often (80–99%) | In 1 condition |
| KLHL10kelch like family member 10 | Very often (80–99%) | In 1 condition |
| LARS2leucyl-tRNA synthetase 2, mitochondrial | Very often (80–99%) | In 1 condition |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | 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 |
| MRPS22mitochondrial ribosomal protein S22 | Very often (80–99%) | In 1 condition |
| MSH4mutS homolog 4 | 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 |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Very often (80–99%) | In 1 condition |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Very often (80–99%) | In 3 conditions |
| NUP107nucleoporin 107 | 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 |
| POLR3HRNA polymerase III subunit H | Very often (80–99%) | In 1 condition |
| PSMC3IPPSMC3 interacting protein | Very often (80–99%) | In 1 condition |
| RBBP7RB binding protein 7, chromatin remodeling factor | 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 |
| SOX9SRY-box transcription factor 9 | Very often (80–99%) | In 1 condition |
Show 27 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| SPAG17sperm associated antigen 17 | Very often (80–99%) | In 1 condition |
| SPIDRscaffold protein involved in DNA repair | Very often (80–99%) | In 1 condition |
| SPINK2serine peptidase inhibitor Kazal type 2 | Very often (80–99%) | In 1 condition |
| SRYsex determining region Y | Very often (80–99%) | In 2 conditions |
| 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 |
| 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 |
| VAMP7vesicle associated membrane protein 7 | Very often (80–99%) | In 1 condition |
| WT1WT1 transcription factor | Very often (80–99%) | In 2 conditions |
| WWOXWW domain containing oxidoreductase | Very often (80–99%) | In 1 condition |
| XRCC2X-ray repair cross complementing 2 | Very often (80–99%) | In 1 condition |
| ZFPM2zinc finger protein, FOG family member 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 2 conditions |
| POLA1DNA polymerase alpha 1, catalytic subunit | Often (30–79%) | In 1 condition |
| CDH23cadherin related 23 | Sometimes (5–29%) | In 1 condition |
| FMR1fragile X messenger ribonucleoprotein 1 | Not recorded | In 1 condition |
| FOXL2forkhead box L2 | Not recorded | In 1 condition |
| HSD17B4hydroxysteroid 17-beta dehydrogenase 4 | Not recorded | In 1 condition |
| LHCGRluteinizing hormone/choriogonadotropin receptor | 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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