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Træk
Increased circulating gonadotropin level
Overproduction of gonadotropins (FSH, LH) by the anterior pituitary gland.
Resumé
- Også kaldet
- Elevated gonadotropins, Elevated serum gonadotropins, Gonadotropin excess
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Denne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/increased-circulating-gonadotropin-level.json"
page <- fromJSON(url)
page$trait$nameIncreased circulating gonadotropin levelHP:0000837
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Læs de gener, der er knyttet til Increased circulating gonadotropin level, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test31 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.
- Female InfertilityReads 19 of these genesBMP15BNC1FANCMFIGLAFSHRLARS2About this report →
- Male InfertilityReads 15 of these genesCFTRDNAH10DNHD1FANCMGCNAMEIOBAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 9 of these genesDHHDHX37GATA4MAP3K1NR5A1SRYAbout this report →
- 46,XX Differences of Sex DevelopmentReads 2 of these genesNR5A1SRYAbout this report →
Show 27 more reports
- Campomelic DysplasiaReads 1 of these genesSOX9About this report →
- Cystic FibrosisReads 1 of these genesCFTRAbout this report →
- FANCM-Related Genomic Instability DisorderReads 1 of these genesFANCMAbout this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- Polycystic Ovary SyndromeReads 1 of these genesFSHRAbout this report →
- Hypertrophic CardiomyopathyReads 6 of these genesDHHDHX37MAP3K1NR5A1SRYZFPM2About this report →
- Hereditary Wilms TumourReads 1 of these genesWT1About this report →
- Congenital Diaphragmatic Hernia (Monogenic)Reads 1 of these genesZFPM2About this report →
- Monogenic Precocious PubertyReads 1 of these genesLHCGRAbout this report →
- Tetralogy of FallotReads 1 of these genesZFPM2About this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 1 of these genesHSD17B4About this report →
- Congenital Adrenal HyperplasiaReads 1 of these genesCYP17A1About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR0B1About this report →
- Usher SyndromeReads 1 of these genesCDH23About this report →
- Type I InterferonopathiesReads 1 of these genesPOLA1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesGATA4About this report →
- Neonatal Diabetes MellitusReads 1 of these genesGATA4About this report →
- Nephrotic SyndromeReads 1 of these genesNUP107About this report →
- Diabetes MellitusReads 1 of these genesGATA4About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesPOLA1About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesNR0B1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesWWOXAbout this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesWWOXFMR1About this report →
- Hearing Loss and DeafnessReads 1 of these genesCDH23About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesMRPS22About this report →
- Epilepsy (Full Panel)Reads 1 of these genesWWOXAbout this report →
- Intellectual DisabilityReads 1 of these genesPOLA1About this report →
Læs de gener, der er knyttet til Increased circulating gonadotropin level, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test67 gener knyttet til Increased circulating gonadotropin level
Ændringer i disse gener forårsager sjældne tilstande, hvor Increased circulating gonadotropin level ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| BMP15bone morphogenetic protein 15 | Meget ofte (80–99 %) | I 1 tilstand |
| BNC1basonuclin zinc finger protein 1 | Meget ofte (80–99 %) | I 1 tilstand |
| CATIPciliogenesis associated TTC17 interacting protein | Meget ofte (80–99 %) | I 1 tilstand |
| CCDC34coiled-coil domain containing 34 | Meget ofte (80–99 %) | I 1 tilstand |
| CFTRCF transmembrane conductance regulator | Meget ofte (80–99 %) | I 1 tilstand |
| CT55cancer/testis antigen 55 | Meget ofte (80–99 %) | I 1 tilstand |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Meget ofte (80–99 %) | I 1 tilstand |
| DHHdesert hedgehog signaling molecule | Meget ofte (80–99 %) | I 1 tilstand |
| DHX37DEAH-box helicase 37 | Meget ofte (80–99 %) | I 1 tilstand |
| DNAH10dynein axonemal heavy chain 10 | Meget ofte (80–99 %) | I 1 tilstand |
| DNHD1dynein heavy chain domain 1 | Meget ofte (80–99 %) | I 1 tilstand |
| ESR1estrogen receptor 1 | Meget ofte (80–99 %) | I 1 tilstand |
| FANCMFA complementation group M | Meget ofte (80–99 %) | I 1 tilstand |
| FBXO43F-box protein 43 | Meget ofte (80–99 %) | I 1 tilstand |
| FIGLAfolliculogenesis specific bHLH transcription factor | Meget ofte (80–99 %) | I 1 tilstand |
| FSHRfollicle stimulating hormone receptor | Meget ofte (80–99 %) | I 3 tilstande |
| GATA4GATA binding protein 4 | Meget ofte (80–99 %) | I 1 tilstand |
| GCNAgerm cell nuclear acidic peptidase | Meget ofte (80–99 %) | I 1 tilstand |
| KLHL10kelch like family member 10 | Meget ofte (80–99 %) | I 1 tilstand |
| LARS2leucyl-tRNA synthetase 2, mitochondrial | Meget ofte (80–99 %) | I 1 tilstand |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| MEIOBmeiosis specific with OB-fold | Meget ofte (80–99 %) | I 1 tilstand |
| MOV10L1Mov10 like RNA helicase 1 | Meget ofte (80–99 %) | I 1 tilstand |
| MRPS22mitochondrial ribosomal protein S22 | Meget ofte (80–99 %) | I 1 tilstand |
| MSH4mutS homolog 4 | Meget ofte (80–99 %) | I 1 tilstand |
| MSH5mutS homolog 5 | Meget ofte (80–99 %) | I 1 tilstand |
| NANOS1nanos C2HC-type zinc finger 1 | Meget ofte (80–99 %) | I 1 tilstand |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Meget ofte (80–99 %) | I 1 tilstand |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Meget ofte (80–99 %) | I 3 tilstande |
| NUP107nucleoporin 107 | Meget ofte (80–99 %) | I 1 tilstand |
| PDHA2pyruvate dehydrogenase E1 subunit alpha 2 | Meget ofte (80–99 %) | I 1 tilstand |
| PNLDC1PARN like ribonuclease domain containing exonuclease 1 | Meget ofte (80–99 %) | I 1 tilstand |
| POLR3HRNA polymerase III subunit H | Meget ofte (80–99 %) | I 1 tilstand |
| PSMC3IPPSMC3 interacting protein | Meget ofte (80–99 %) | I 1 tilstand |
| RBBP7RB binding protein 7, chromatin remodeling factor | Meget ofte (80–99 %) | I 1 tilstand |
| RNF212ring finger protein 212 | Meget ofte (80–99 %) | I 1 tilstand |
| RPL10Lribosomal protein L10 like | Meget ofte (80–99 %) | I 1 tilstand |
| SHOC1shortage in chiasmata 1 | Meget ofte (80–99 %) | I 1 tilstand |
| SOHLH1spermatogenesis and oogenesis specific basic helix-loop-helix 1 | Meget ofte (80–99 %) | I 1 tilstand |
| SOX9SRY-box transcription factor 9 | Meget ofte (80–99 %) | I 1 tilstand |
Vis 27 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| SPAG17sperm associated antigen 17 | Meget ofte (80–99 %) | I 1 tilstand |
| SPIDRscaffold protein involved in DNA repair | Meget ofte (80–99 %) | I 1 tilstand |
| SPINK2serine peptidase inhibitor Kazal type 2 | Meget ofte (80–99 %) | I 1 tilstand |
| SRYsex determining region Y | Meget ofte (80–99 %) | I 2 tilstande |
| STAG3STAG3 cohesin complex component | Meget ofte (80–99 %) | I 1 tilstand |
| SYCE1synaptonemal complex central element protein 1 | Meget ofte (80–99 %) | I 1 tilstand |
| SYCP3synaptonemal complex protein 3 | Meget ofte (80–99 %) | I 1 tilstand |
| TAF4BTATA-box binding protein associated factor 4b | Meget ofte (80–99 %) | I 1 tilstand |
| TDRD9tudor domain containing 9 | Meget ofte (80–99 %) | I 1 tilstand |
| TERB1telomere repeat binding bouquet formation protein 1 | Meget ofte (80–99 %) | I 1 tilstand |
| TERB2telomere repeat binding bouquet formation protein 2 | Meget ofte (80–99 %) | I 1 tilstand |
| TEX11testis expressed 11 | Meget ofte (80–99 %) | I 1 tilstand |
| TEX14testis expressed 14, intercellular bridge forming factor | Meget ofte (80–99 %) | I 1 tilstand |
| TEX15testis expressed 15, meiosis and synapsis associated | Meget ofte (80–99 %) | I 1 tilstand |
| VAMP7vesicle associated membrane protein 7 | Meget ofte (80–99 %) | I 1 tilstand |
| WT1WT1 transcription factor | Meget ofte (80–99 %) | I 2 tilstande |
| WWOXWW domain containing oxidoreductase | Meget ofte (80–99 %) | I 1 tilstand |
| XRCC2X-ray repair cross complementing 2 | Meget ofte (80–99 %) | I 1 tilstand |
| ZFPM2zinc finger protein, FOG family member 2 | Meget ofte (80–99 %) | I 1 tilstand |
| ZMYND15zinc finger MYND-type containing 15 | Meget ofte (80–99 %) | I 1 tilstand |
| ZSWIM7zinc finger SWIM-type containing 7 | Meget ofte (80–99 %) | I 2 tilstande |
| POLA1DNA polymerase alpha 1, catalytic subunit | Ofte (30–79 %) | I 1 tilstand |
| CDH23cadherin related 23 | Nogle gange (5–29 %) | I 1 tilstand |
| FMR1fragile X messenger ribonucleoprotein 1 | Ikke registreret | I 1 tilstand |
| FOXL2forkhead box L2 | Ikke registreret | I 1 tilstand |
| HSD17B4hydroxysteroid 17-beta dehydrogenase 4 | Ikke registreret | I 1 tilstand |
| LHCGRluteinizing hormone/choriogonadotropin receptor | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Snævrere træk
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
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