AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Özellik
Decreased activity of gonads
Klinik adı: Hypogonadism
A decreased functionality of the gonad.
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Bu sayfanın veri olarak görünümü
Veriyi JSON olarak okumak için sayfa adresinin sonuna .json ekleyin veya application/json isteyin.
library(jsonlite)
url <- "https://dantelabs.com/traits/hypogonadism.json"
page <- fromJSON(url)
page$trait$nameDecreased activity of gonadsHP:0000135
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Decreased activity of gonads ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi al114 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.
- Bardet-Biedl and Alström SyndromesReads 22 of these genesBBS12BBS2BBS5BBS7IFT74LZTFL1About this report →
- Fanconi AnemiaReads 18 of these genesFANCBERCC4BRCA1BRCA2BRIP1FANCAAbout this report →
- DNA Repair DiseaseReads 27 of these genesFANCBDDB2ERCC2ERCC3ERCC4ERCC5About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 3 of these genesPDE4DPRKAR1AGNASAbout this report →
Show 110 more reports
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Myotonic DystrophyReads 2 of these genesCNBPDMPKAbout this report →
- Wolfram Syndrome & WFS1 SpectrumReads 2 of these genesCISD2WFS1About this report →
- Hypogonadotropic HypogonadismReads 10 of these genesDCAF17FEZF1RNF216SMCHD1MAGEL2SEMA3AAbout this report →
- Rothmund-Thomson SyndromeReads 2 of these genesANAPC1RECQL4About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 3 of these genesSIM1CEP19LEPAbout this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 3 of these genesBRIP1PALB2RAD51CAbout this report →
- Androgen Insensitivity SyndromeReads 1 of these genesARAbout this report →
- Autoimmune Polyendocrine Syndrome Type 1 (APECED)Reads 1 of these genesAIREAbout this report →
- Björnstad SyndromeReads 1 of these genesBCS1LAbout this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- CHRNG-Related Multiple Pterygium SyndromeReads 1 of these genesCHRNGAbout this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- Dias-Logan SyndromeReads 1 of these genesBCL11AAbout this report →
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- FANCM-Related Genomic Instability DisorderReads 1 of these genesFANCMAbout this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- Frontonasal Dysplasia with Alopecia and Genital Anomaly (ALX4)Reads 1 of these genesALX4About this report →
- GAPO SyndromeReads 1 of these genesANTXR1About this report →
- H SyndromeReads 1 of these genesSLC29A3About this report →
- Hao-Fountain SyndromeReads 1 of these genesUSP7About this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- OPA1-Related Optic AtrophyReads 1 of these genesOPA1About this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- PNPLA6-Related Ataxia, Retinal Dystrophy and HypogonadismReads 1 of these genesPNPLA6About this report →
- Primrose SyndromeReads 1 of these genesZBTB20About this report →
- Radio-Tartaglia SyndromeReads 1 of these genesSPENAbout this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- Sickle Cell DiseaseReads 1 of these genesHBBAbout this report →
- Spinal and Bulbar Muscular Atrophy (Kennedy Disease)Reads 1 of these genesARAbout this report →
- Werner SyndromeReads 1 of these genesWRNAbout this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- X-Linked Chondrodysplasia Punctata 1Reads 1 of these genesARSLAbout this report →
- HemochromatosisReads 2 of these genesHAMPHJVAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 6 of these genesPEX6SIL1CEP290MKS1STUB1TWNKAbout this report →
- Inherited Neurodegenerative DisordersReads 15 of these genesDCAF17PNPLA6FMR1PEX1PEX6RNF216About this report →
- Malignant Endocrine NeoplasmReads 2 of these genesTP53MEN1About this report →
- Acrodermatitis EnteropathicaReads 1 of these genesSLC39A4About this report →
- CystinuriaReads 1 of these genesSLC3A1About this report →
- Encephalopathy due to Mitochondrial and Peroxisomal Fission DefectReads 1 of these genesDNM1LAbout this report →
- Enlarged Parietal Foramina (MSX2)Reads 1 of these genesALX4About this report →
- Familial Isolated Pituitary Adenoma (FIPA / X-LAG)Reads 1 of these genesAIPAbout this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 3 of these genesNPHP1SDCCAG8IFT54About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 2 of these genesCDKN1CMAGEL2About this report →
- Noonan SyndromeReads 3 of these genesBRAFMAP2K1PTPN11About this report →
- Hypertrophic CardiomyopathyReads 5 of these genesCDKN1CBRAFMAP2K1PTPN11DMPKAbout this report →
- Marfan Like SyndromesReads 2 of these genesSKITGFB2About this report →
- Primary Mitochondrial DiseaseReads 7 of these genesATP5F1AATP5F1DATP5F1EATP5POBCS1LTWNKAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 3 of these genesERCC2ERCC5ERCC1About this report →
- Retinitis PigmentosaReads 5 of these genesBBS2TTC8ARL6CFAP418IFT172About this report →
- Hereditary Optic NeuropathyReads 2 of these genesDNM1LOPA1About this report →
- Thyroid CancerReads 3 of these genesMEN1AIREGNASAbout this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 2 of these genesPEX1PEX6About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 1 of these genesREREAbout this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Joubert Syndrome And Related DisordersReads 3 of these genesCEP290MKS1NPHP1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 2 of these genesARATRXAbout this report →
- Intellectual DisabilityReads 7 of these genesPHF6CTNNB1SCAPERCUL4BSMAD4MYT1LAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 1 of these genesHBBAbout this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesTGFB1About this report →
- ThalassaemiaReads 1 of these genesHBBAbout this report →
- Autoimmune DiseaseReads 2 of these genesAIRECHRNGAbout this report →
- Syndromic CraniosynostosisReads 2 of these genesSKIRECQL4About this report →
- Female InfertilityReads 3 of these genesFMR1FANCMTWNKAbout this report →
- Cornelia de Lange SyndromeReads 1 of these genesHDAC8About this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesIGF1About this report →
- Hereditary SpherocytosisReads 1 of these genesANK1About this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesTGFB1About this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFB2About this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 1 of these genesAMACRAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 6 of these genesLMNAPEX1PEX6ATP5MKMT-ATP6OPA1About this report →
- Colorectal Cancer & PolyposisReads 1 of these genesPOLEAbout this report →
- Waardenburg SyndromeReads 1 of these genesSOX10About this report →
- Leigh SyndromeReads 3 of these genesATP5MKMT-ATP6OPA1About this report →
- Disorders of Glycine & Serine MetabolismReads 1 of these genesPHGDHAbout this report →
- PolycythemiaReads 1 of these genesHBBAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesLMNATRIM32About this report →
- Other Inherited LeukodystrophiesReads 3 of these genesPEX1PEX6ABCD1About this report →
- Kidney CancerReads 1 of these genesTP53About this report →
- Meckel SyndromeReads 1 of these genesMKS1About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesDCAF17About this report →
- Usher SyndromeReads 1 of these genesCDH23About this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Urinary and Renal System TumourReads 1 of these genesTP53About this report →
- Dilated CardiomyopathyReads 2 of these genesLMNAPRDM16About this report →
- Aortic AneurysmReads 1 of these genesTGFB2About this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesPNPLA6ABCD1About this report →
- Ectodermal DysplasiasReads 1 of these genesNECTIN1About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 1 of these genesCEP290About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesWFS1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesMYT1LAbout this report →
- Inherited IchthyosesReads 1 of these genesSTSAbout this report →
- Hearing Loss and DeafnessReads 2 of these genesCDH23WFS1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesPROP1About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesPREPLAbout this report →
- VitreoretinopathyReads 1 of these genesCTNNB1About this report →
- Nephrotic SyndromeReads 1 of these genesSGPL1About this report →
- Diabetes MellitusReads 1 of these genesZBTB20About this report →
- Osteogenesis ImperfectaReads 1 of these genesPPIBAbout this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesSNAP29About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesSTUB1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesDCAF17About this report →
- Male InfertilityReads 1 of these genesFANCMAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Congenital Disorders of GlycosylationReads 1 of these genesALG1About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesRELAbout this report →
Decreased activity of gonads ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi alDecreased activity of gonads ile ilişkili 171 gen
Bu genlerdeki değişiklikler, Decreased activity of gonads özelliğinin görüldüğü nadir durumlara yol açar. Bu özelliğe sahip çoğu kişide bu durumlardan hiçbiri yoktur; ayrıca bu listedeki bir gen, kimsenin kendi genomu hakkında bir şey söylemez.
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| ALG1ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Her zaman | 1 durumda |
| BBS12Bardet-Biedl syndrome 12 | Her zaman | 2 durumda |
| BBS2Bardet-Biedl syndrome 2 | Her zaman | 2 durumda |
| BBS5Bardet-Biedl syndrome 5 | Her zaman | 2 durumda |
| BBS7Bardet-Biedl syndrome 7 | Her zaman | 2 durumda |
| DCAF17DDB1 and CUL4 associated factor 17 | Her zaman | 2 durumda |
| FANCBFA complementation group B | Her zaman | 2 durumda |
| FEZF1FEZ family zinc finger 1 | Her zaman | 1 durumda |
| HAMPhepcidin antimicrobial peptide | Her zaman | 2 durumda |
| IFT74intraflagellar transport 74 | Her zaman | 2 durumda |
| LZTFL1leucine zipper transcription factor like 1 | Her zaman | 2 durumda |
| MDM2MDM2 proto-oncogene | Her zaman | 1 durumda |
| PNPLA6patatin like domain 6, lysophospholipase | Her zaman | 3 durumda |
| SLC30A7solute carrier family 30 member 7 | Her zaman | 1 durumda |
| STEAP3STEAP3 metalloreductase | Her zaman | 2 durumda |
| TP53tumor protein p53 | Her zaman | 1 durumda |
| AIPAHR interacting HSP90 co-chaperone | Çok sık (%80–99) | 1 durumda |
| ALX4ALX homeobox 4 | Çok sık (%80–99) | 1 durumda |
| ANK1ankyrin 1 | Çok sık (%80–99) | 1 durumda |
| CAMKMTcalmodulin-lysine N-methyltransferase | Çok sık (%80–99) | 1 durumda |
| CDH23cadherin related 23 | Çok sık (%80–99) | 2 durumda |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Çok sık (%80–99) | 1 durumda |
| DDB2damage specific DNA binding protein 2 | Çok sık (%80–99) | 1 durumda |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Çok sık (%80–99) | 3 durumda |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Çok sık (%80–99) | 2 durumda |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Çok sık (%80–99) | 2 durumda |
| ERCC5ERCC excision repair 5, endonuclease | Çok sık (%80–99) | 2 durumda |
| FMR1fragile X messenger ribonucleoprotein 1 | Çok sık (%80–99) | 1 durumda |
| LMNAlamin A/C | Çok sık (%80–99) | 1 durumda |
| MEN1menin 1 | Çok sık (%80–99) | 1 durumda |
| PEX1peroxisomal biogenesis factor 1 | Çok sık (%80–99) | 1 durumda |
| PEX6peroxisomal biogenesis factor 6 | Çok sık (%80–99) | 1 durumda |
| PHF6PHD finger protein 6 | Çok sık (%80–99) | 1 durumda |
| POLEDNA polymerase epsilon, catalytic subunit | Çok sık (%80–99) | 1 durumda |
| PPM1Bprotein phosphatase, Mg2+/Mn2+ dependent 1B | Çok sık (%80–99) | 1 durumda |
| PREPLprolyl endopeptidase like | Çok sık (%80–99) | 1 durumda |
| RNF216ring finger protein 216 | Çok sık (%80–99) | 1 durumda |
| SIL1SIL1 nucleotide exchange factor | Çok sık (%80–99) | 1 durumda |
| SIM1SIM bHLH transcription factor 1 | Çok sık (%80–99) | 1 durumda |
| SLC3A1solute carrier family 3 member 1 | Çok sık (%80–99) | 1 durumda |
131 gen daha göster
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Çok sık (%80–99) | 1 durumda |
| TTC8tetratricopeptide repeat domain 8 | Çok sık (%80–99) | 2 durumda |
| WRNWRN RecQ like helicase | Çok sık (%80–99) | 2 durumda |
| XPAXPA, DNA damage recognition and repair factor | Çok sık (%80–99) | 1 durumda |
| XPCXPC complex subunit, DNA damage recognition and repair factor | Çok sık (%80–99) | 1 durumda |
| ZBTB20zinc finger and BTB domain containing 20 | Çok sık (%80–99) | 1 durumda |
| AIREautoimmune regulator | Sık (%30–79) | 2 durumda |
| ARL6ARF like GTPase 6 | Sık (%30–79) | 2 durumda |
| BBIP1BBSome interacting protein 1 | Sık (%30–79) | 1 durumda |
| BBS1Bardet-Biedl syndrome 1 | Sık (%30–79) | 2 durumda |
| BBS10Bardet-Biedl syndrome 10 | Sık (%30–79) | 2 durumda |
| BBS4Bardet-Biedl syndrome 4 | Sık (%30–79) | 2 durumda |
| BBS9Bardet-Biedl syndrome 9 | Sık (%30–79) | 1 durumda |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Sık (%30–79) | 2 durumda |
| CEP19centrosomal protein 19 | Sık (%30–79) | 1 durumda |
| CEP290centrosomal protein 290 | Sık (%30–79) | 1 durumda |
| CFAP418cilia and flagella associated protein 418 | Sık (%30–79) | 1 durumda |
| CHRNGcholinergic receptor nicotinic gamma subunit | Sık (%30–79) | 1 durumda |
| CTNNB1catenin beta 1 | Sık (%30–79) | 1 durumda |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Sık (%30–79) | 1 durumda |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Sık (%30–79) | 1 durumda |
| HJVhemojuvelin BMP co-receptor | Sık (%30–79) | 1 durumda |
| IFT172intraflagellar transport 172 | Sık (%30–79) | 1 durumda |
| IFT27intraflagellar transport 27 | Sık (%30–79) | 2 durumda |
| IGF1insulin like growth factor 1 | Sık (%30–79) | 1 durumda |
| MAGEL2MAGE family member L2 | Sık (%30–79) | 2 durumda |
| MKKSMKKS centrosomal shuttling protein | Sık (%30–79) | 1 durumda |
| MKS1MKS transition zone complex subunit 1 | Sık (%30–79) | 1 durumda |
| MYH3myosin heavy chain 3 | Sık (%30–79) | 1 durumda |
| NECTIN1nectin cell adhesion molecule 1 | Sık (%30–79) | 1 durumda |
| NPHP1nephrocystin 1 | Sık (%30–79) | 1 durumda |
| SCAPERS-phase cyclin A associated protein in the ER | Sık (%30–79) | 1 durumda |
| SCLT1sodium channel and clathrin linker 1 | Sık (%30–79) | 1 durumda |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Sık (%30–79) | 2 durumda |
| SEMA3Asemaphorin 3A | Sık (%30–79) | 1 durumda |
| SOX10SRY-box transcription factor 10 | Sık (%30–79) | 2 durumda |
| TRIM32tripartite motif containing 32 | Sık (%30–79) | 2 durumda |
| USP7ubiquitin specific peptidase 7 | Sık (%30–79) | 1 durumda |
| WDPCPWD repeat containing planar cell polarity effector | Sık (%30–79) | 1 durumda |
| AMACRalpha-methylacyl-CoA racemase | Bazen (%5–29) | 1 durumda |
| ANAPC1anaphase promoting complex subunit 1 | Bazen (%5–29) | 1 durumda |
| ANTXR1ANTXR cell adhesion molecule 1 | Bazen (%5–29) | 1 durumda |
| ATP5F1AATP synthase F1 subunit alpha | Bazen (%5–29) | 1 durumda |
| ATP5F1DATP synthase F1 subunit delta | Bazen (%5–29) | 1 durumda |
| ATP5F1EATP synthase F1 subunit epsilon | Bazen (%5–29) | 1 durumda |
| ATP5MKATP synthase membrane subunit k | Bazen (%5–29) | 1 durumda |
| ATP5POATP synthase peripheral stalk subunit OSCP | Bazen (%5–29) | 1 durumda |
| ATPAF2ATP synthase mitochondrial F1 complex assembly factor 2 | Bazen (%5–29) | 1 durumda |
| BCL11ABCL11 transcription factor A | Bazen (%5–29) | 1 durumda |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Bazen (%5–29) | 1 durumda |
| BRCA1BRCA1 DNA repair associated | Bazen (%5–29) | 1 durumda |
| BRCA2BRCA2 DNA repair associated | Bazen (%5–29) | 1 durumda |
| BRIP1BRCA1 interacting DNA helicase 1 | Bazen (%5–29) | 1 durumda |
| CASZ1castor zinc finger 1 | Bazen (%5–29) | 1 durumda |
| CISD2CDGSH iron sulfur domain 2 | Bazen (%5–29) | 1 durumda |
| CUL4Bcullin 4B | Bazen (%5–29) | 2 durumda |
| FAAP100FA core complex associated protein 100 | Bazen (%5–29) | 1 durumda |
| FANCAFA complementation group A | Bazen (%5–29) | 1 durumda |
| FANCCFA complementation group C | Bazen (%5–29) | 1 durumda |
| FANCD2FA complementation group D2 | Bazen (%5–29) | 1 durumda |
| FANCEFA complementation group E | Bazen (%5–29) | 1 durumda |
| FANCFFA complementation group F | Bazen (%5–29) | 1 durumda |
| FANCGFA complementation group G | Bazen (%5–29) | 1 durumda |
| FANCIFA complementation group I | Bazen (%5–29) | 1 durumda |
| FANCLFA complementation group L | Bazen (%5–29) | 1 durumda |
| FANCMFA complementation group M | Bazen (%5–29) | 1 durumda |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Bazen (%5–29) | 1 durumda |
| HSPG2heparan sulfate proteoglycan 2 | Bazen (%5–29) | 1 durumda |
| IER3IP1immediate early response 3 interacting protein 1 | Bazen (%5–29) | 1 durumda |
| IFT54intraflagellar transport 54 | Bazen (%5–29) | 1 durumda |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Bazen (%5–29) | 1 durumda |
| LUZP1leucine zipper protein 1 | Bazen (%5–29) | 1 durumda |
| MAD2L2mitotic arrest deficient 2 like 2 | Bazen (%5–29) | 1 durumda |
| MAP2K1mitogen-activated protein kinase kinase 1 | Bazen (%5–29) | 1 durumda |
| MMP23Bmatrix metallopeptidase 23B | Bazen (%5–29) | 1 durumda |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Bazen (%5–29) | 1 durumda |
| MT-ATP8mitochondrially encoded ATP synthase membrane subunit 8 | Bazen (%5–29) | 1 durumda |
| PALB2partner and localizer of BRCA2 | Bazen (%5–29) | 1 durumda |
| PDE4Dphosphodiesterase 4D | Bazen (%5–29) | 1 durumda |
| PDPNpodoplanin | Bazen (%5–29) | 1 durumda |
| PHGDHphosphoglycerate dehydrogenase | Bazen (%5–29) | 1 durumda |
| PRDM16PR/SET domain 16 | Bazen (%5–29) | 1 durumda |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Bazen (%5–29) | 2 durumda |
| PRKCZprotein kinase C zeta | Bazen (%5–29) | 1 durumda |
| PTDSS1phosphatidylserine synthase 1 | Bazen (%5–29) | 1 durumda |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Bazen (%5–29) | 1 durumda |
| RAD51RAD51 recombinase | Bazen (%5–29) | 1 durumda |
| RAD51CRAD51 paralog C | Bazen (%5–29) | 1 durumda |
| RELREL proto-oncogene, NF-kB subunit | Bazen (%5–29) | 1 durumda |
| REREarginine-glutamic acid dipeptide repeats | Bazen (%5–29) | 1 durumda |
| RFWD3ring finger and WD repeat domain 3 | Bazen (%5–29) | 1 durumda |
| SKISKI proto-oncogene | Bazen (%5–29) | 1 durumda |
| SLC29A3solute carrier family 29 member 3 | Bazen (%5–29) | 1 durumda |
| SLX4SLX4 structure-specific endonuclease subunit | Bazen (%5–29) | 1 durumda |
| SMAD4SMAD family member 4 | Bazen (%5–29) | 1 durumda |
| SNAP29synaptosome associated protein 29 | Bazen (%5–29) | 1 durumda |
| SPENspen family transcriptional repressor | Bazen (%5–29) | 1 durumda |
| STSsteroid sulfatase | Bazen (%5–29) | 1 durumda |
| STUB1STIP1 homology and U-box containing protein 1 | Bazen (%5–29) | 2 durumda |
| TGFB1transforming growth factor beta 1 | Bazen (%5–29) | 1 durumda |
| TWNKtwinkle mtDNA helicase | Bazen (%5–29) | 1 durumda |
| UBE2Tubiquitin conjugating enzyme E2 T | Bazen (%5–29) | 1 durumda |
| UBE4Bubiquitination factor E4B | Bazen (%5–29) | 1 durumda |
| VPS4Avacuolar protein sorting 4 homolog A | Bazen (%5–29) | 1 durumda |
| WFS1wolframin ER transmembrane glycoprotein | Bazen (%5–29) | 1 durumda |
| XPO1exportin 1 | Bazen (%5–29) | 1 durumda |
| XRCC2X-ray repair cross complementing 2 | Bazen (%5–29) | 1 durumda |
| DNM1Ldynamin 1L | Seyrek (%1–4) | 1 durumda |
| HBBhemoglobin subunit beta | Seyrek (%1–4) | 1 durumda |
| MYT1Lmyelin transcription factor 1 like | Seyrek (%1–4) | 1 durumda |
| OPA1OPA1 mitochondrial dynamin like GTPase | Seyrek (%1–4) | 1 durumda |
| PPIBpeptidylprolyl isomerase B | Seyrek (%1–4) | 1 durumda |
| ABCD1ATP binding cassette subfamily D member 1 | Kaydedilmedi | 1 durumda |
| ARandrogen receptor | Kaydedilmedi | 1 durumda |
| ARSLarylsulfatase L | Kaydedilmedi | 1 durumda |
| ATRXATRX chromatin remodeler | Kaydedilmedi | 1 durumda |
| CCDC28Bcoiled-coil domain containing 28B | Kaydedilmedi | 1 durumda |
| CNBPCCHC-type zinc finger nucleic acid binding protein | Kaydedilmedi | 1 durumda |
| DMPKDM1 protein kinase | Kaydedilmedi | 1 durumda |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Kaydedilmedi | 1 durumda |
| FGF17fibroblast growth factor 17 | Kaydedilmedi | 1 durumda |
| FSHBfollicle stimulating hormone subunit beta | Kaydedilmedi | 1 durumda |
| GNASGNAS complex locus | Kaydedilmedi | 2 durumda |
| HDAC8histone deacetylase 8 | Kaydedilmedi | 1 durumda |
| IL17RDinterleukin 17 receptor D | Kaydedilmedi | 1 durumda |
| LEPleptin | Kaydedilmedi | 1 durumda |
| PROP1PROP paired-like homeobox 1 | Kaydedilmedi | 1 durumda |
| RECQL4RecQ like helicase 4 | Kaydedilmedi | 1 durumda |
| SGPL1sphingosine-1-phosphate lyase 1 | Kaydedilmedi | 1 durumda |
| SLC39A4solute carrier family 39 member 4 | Kaydedilmedi | 1 durumda |
| TGFB2transforming growth factor beta 2 | Kaydedilmedi | 1 durumda |
Bu özelliğin, genin ilişkili olduğu durumlardan birine sahip kişiler arasında ne sıklıkta görüldüğü; Human Phenotype Ontology'nin kaydettiği şekliyle, bunlar arasında en sık görülen oran. Bu sayfalar özellikleri ve bunların arkasındaki araştırmaları anlatır; tanı koymaz. Belirtiler hakkında bir doktora veya genetik danışmana başvurmanız gerekir.
Daha dar özellikler
Daha geniş özellikler
Bilgilerin kaynağı
- Human Phenotype Ontology, 2026-09-01 sürümü: özellik, adları, tanımı ve buna bağlı genler. Ayrıntılar için hpo.jax.org adresine bakın.
- Veri sürümü 2026.10.18-8b139e39.
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