Tunnus
Delayed puberty
Passing the age when puberty normally occurs with no physical or hormonal signs of the onset of puberty.
Kokkuvõte
- Teised nimetused
- Delayed pubertal development, Delayed pubertal growth, Pubertal delay
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Delayed puberty, and the rest of your genome, with one test.
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Telli oma Genome Test199 geeni on seotud tunnusega Delayed puberty
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Delayed puberty. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| BMP15bone morphogenetic protein 15 | Alati | Esineb 2 haiguses |
| BTKBruton tyrosine kinase | Alati | Esineb 1 haiguses |
| DCAF17DDB1 and CUL4 associated factor 17 | Alati | Esineb 2 haiguses |
| ESR1estrogen receptor 1 | Alati | Esineb 1 haiguses |
| FAM111BFAM111 trypsin like peptidase B | Alati | Esineb 1 haiguses |
| GTF3C3general transcription factor IIIC subunit 3 | Alati | Esineb 1 haiguses |
| HROBhomologous recombination factor with OB-fold | Alati | Esineb 1 haiguses |
| LEPRleptin receptor | Alati | Esineb 1 haiguses |
| PRDM13PR/SET domain 13 | Alati | Esineb 1 haiguses |
| PSMC3IPPSMC3 interacting protein | Alati | Esineb 2 haiguses |
| RBM28RNA binding motif protein 28 | Alati | Esineb 2 haiguses |
| RNU2-2RNA, U2 small nuclear 2 | Alati | Esineb 1 haiguses |
| RNU6ATACRNA, U6atac small nuclear | Alati | Esineb 1 haiguses |
| SPIDRscaffold protein involved in DNA repair | Alati | Esineb 2 haiguses |
| TAF13TATA-box binding protein associated factor 13 | Alati | Esineb 1 haiguses |
| TRA2Btransformer 2 beta homolog | Alati | Esineb 1 haiguses |
| ZSWIM7zinc finger SWIM-type containing 7 | Alati | Esineb 2 haiguses |
| ANOS1anosmin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ATMATM serine/threonine kinase | Väga sageli (80–99%) | Esineb 2 haiguses |
| BNC1basonuclin zinc finger protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CCDC141coiled-coil domain containing 141 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CHD7chromodomain helicase DNA binding protein 7 | Väga sageli (80–99%) | Esineb 4 haiguses |
| CYB5Acytochrome b5 type A | Väga sageli (80–99%) | Esineb 1 haiguses |
| CYP11A1cytochrome P450 family 11 subfamily A member 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| DCCDCC netrin 1 receptor | Väga sageli (80–99%) | Esineb 1 haiguses |
| DUSP6dual specificity phosphatase 6 | Väga sageli (80–99%) | Esineb 2 haiguses |
| EMX2empty spiracles homeobox 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| FEZF1FEZ family zinc finger 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FGF17fibroblast growth factor 17 | Väga sageli (80–99%) | Esineb 3 haiguses |
| FGF8fibroblast growth factor 8 | Väga sageli (80–99%) | Esineb 3 haiguses |
| FGFR1fibroblast growth factor receptor 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| FIGLAfolliculogenesis specific bHLH transcription factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| FLRT3fibronectin leucine rich transmembrane protein 3 | Väga sageli (80–99%) | Esineb 2 haiguses |
| FSHBfollicle stimulating hormone subunit beta | Väga sageli (80–99%) | Esineb 1 haiguses |
| FSHRfollicle stimulating hormone receptor | Väga sageli (80–99%) | Esineb 1 haiguses |
| GBA1glucosylceramidase beta 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| HESX1HESX homeobox 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| HS6ST1heparan sulfate 6-O-sulfotransferase 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| IL17RDinterleukin 17 receptor D | Väga sageli (80–99%) | Esineb 1 haiguses |
Näita veel 159 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| INSRinsulin receptor | Väga sageli (80–99%) | Esineb 1 haiguses |
| LMNAlamin A/C | Väga sageli (80–99%) | Esineb 1 haiguses |
| MRPS22mitochondrial ribosomal protein S22 | Väga sageli (80–99%) | Esineb 2 haiguses |
| MSH4mutS homolog 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NDNFneuron derived neurotrophic factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| NUP107nucleoporin 107 | Väga sageli (80–99%) | Esineb 1 haiguses |
| POLR3ARNA polymerase III subunit A | Väga sageli (80–99%) | Esineb 2 haiguses |
| POLR3BRNA polymerase III subunit B | Väga sageli (80–99%) | Esineb 1 haiguses |
| POLR3HRNA polymerase III subunit H | Väga sageli (80–99%) | Esineb 1 haiguses |
| PROK2prokineticin 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PROKR2prokineticin receptor 2 | Väga sageli (80–99%) | Esineb 3 haiguses |
| RAB18RAB18, member RAS oncogene family | Väga sageli (80–99%) | Esineb 1 haiguses |
| RAB3GAP1RAB3 GTPase activating protein catalytic subunit 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SCARB2scavenger receptor class B member 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SEMA3Asemaphorin 3A | Väga sageli (80–99%) | Esineb 1 haiguses |
| SEMA3Esemaphorin 3E | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC29A3solute carrier family 29 member 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SOX10SRY-box transcription factor 10 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SPRY4sprouty RTK signaling antagonist 4 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TACR3tachykinin receptor 3 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TBC1D20TBC1 domain family member 20 | Väga sageli (80–99%) | Esineb 1 haiguses |
| WDR11WD repeat domain 11 | Väga sageli (80–99%) | Esineb 3 haiguses |
| ARandrogen receptor | Sageli (30–79%) | Esineb 1 haiguses |
| BRCC3BRCA1/BRCA2-containing complex subunit 3 | Sageli (30–79%) | Esineb 1 haiguses |
| CDONcell adhesion associated, oncogene regulated | Sageli (30–79%) | Esineb 1 haiguses |
| CPEcarboxypeptidase E | Sageli (30–79%) | Esineb 1 haiguses |
| DHX37DEAH-box helicase 37 | Sageli (30–79%) | Esineb 1 haiguses |
| ENTPD1ectonucleoside triphosphate diphosphohydrolase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| GALTgalactose-1-phosphate uridylyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| GATA4GATA binding protein 4 | Sageli (30–79%) | Esineb 1 haiguses |
| GHRgrowth hormone receptor | Sageli (30–79%) | Esineb 2 haiguses |
| GLAgalactosidase alpha | Sageli (30–79%) | Esineb 2 haiguses |
| GNRH1gonadotropin releasing hormone 1 | Sageli (30–79%) | Esineb 2 haiguses |
| GNRHRgonadotropin releasing hormone receptor | Sageli (30–79%) | Esineb 1 haiguses |
| GPR161G protein-coupled receptor 161 | Sageli (30–79%) | Esineb 1 haiguses |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| IGFALSinsulin like growth factor binding protein acid labile subunit | Sageli (30–79%) | Esineb 2 haiguses |
| KISS1KiSS-1 metastasis suppressor | Sageli (30–79%) | Esineb 1 haiguses |
| KISS1RKISS1 receptor | Sageli (30–79%) | Esineb 1 haiguses |
| LHX4LIM homeobox 4 | Sageli (30–79%) | Esineb 2 haiguses |
| LPIN2lipin 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MAGEL2MAGE family member L2 | Sageli (30–79%) | Esineb 4 haiguses |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MKRN3makorin ring finger protein 3 | Sageli (30–79%) | Esineb 1 haiguses |
| NDNnecdin, MAGE family member | Sageli (30–79%) | Esineb 3 haiguses |
| NHLH2nescient helix-loop-helix 2 | Sageli (30–79%) | Esineb 1 haiguses |
| NONOnon-POU domain containing octamer binding | Sageli (30–79%) | Esineb 2 haiguses |
| NPAP1nuclear pore associated protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Sageli (30–79%) | Esineb 3 haiguses |
| NSMFNMDA receptor synaptonuclear signaling and neuronal migration factor | Sageli (30–79%) | Esineb 1 haiguses |
| OCA2OCA2 melanosomal transmembrane protein | Sageli (30–79%) | Esineb 3 haiguses |
| POLR3GLRNA polymerase III subunit GL | Sageli (30–79%) | Esineb 1 haiguses |
| PPP1R15Bprotein phosphatase 1 regulatory subunit 15B | Sageli (30–79%) | Esineb 2 haiguses |
| PUS1pseudouridine synthase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| PWAR1Prader Willi/Angelman region RNA 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PYGLglycogen phosphorylase L | Sageli (30–79%) | Esineb 1 haiguses |
| ROBO1roundabout guidance receptor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SMPD1sphingomyelin phosphodiesterase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Sageli (30–79%) | Esineb 1 haiguses |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Sageli (30–79%) | Esineb 1 haiguses |
| SNRPNsmall nuclear ribonucleoprotein polypeptide N | Sageli (30–79%) | Esineb 3 haiguses |
| SOX11SRY-box transcription factor 11 | Sageli (30–79%) | Esineb 1 haiguses |
| SOX9SRY-box transcription factor 9 | Sageli (30–79%) | Esineb 1 haiguses |
| SRYsex determining region Y | Sageli (30–79%) | Esineb 2 haiguses |
| STAT1signal transducer and activator of transcription 1 | Sageli (30–79%) | Esineb 2 haiguses |
| STAT5Bsignal transducer and activator of transcription 5B | Sageli (30–79%) | Esineb 2 haiguses |
| TAC3tachykinin precursor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| TBX3T-box transcription factor 3 | Sageli (30–79%) | Esineb 2 haiguses |
| TRMT10AtRNA methyltransferase 10A | Sageli (30–79%) | Esineb 2 haiguses |
| VAMP7vesicle associated membrane protein 7 | Sageli (30–79%) | Esineb 1 haiguses |
| VPS13Bvacuolar protein sorting 13 homolog B | Sageli (30–79%) | Esineb 2 haiguses |
| WFS1wolframin ER transmembrane glycoprotein | Sageli (30–79%) | Esineb 2 haiguses |
| WT1WT1 transcription factor | Sageli (30–79%) | Esineb 1 haiguses |
| WWOXWW domain containing oxidoreductase | Sageli (30–79%) | Esineb 1 haiguses |
| YARS2tyrosyl-tRNA synthetase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ZBTB20zinc finger and BTB domain containing 20 | Sageli (30–79%) | Esineb 1 haiguses |
| ZFPM2zinc finger protein, FOG family member 2 | Sageli (30–79%) | Esineb 1 haiguses |
| AIPAHR interacting HSP90 co-chaperone | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALX4ALX homeobox 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATAD3AATPase family AAA domain containing 3A | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRD4bromodomain containing 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CARS1cysteinyl-tRNA synthetase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDH23cadherin related 23 | Mõnikord (5–29%) | Esineb 2 haiguses |
| CISD2CDGSH iron sulfur domain 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CLCNKBchloride voltage-gated channel Kb | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL7A1collagen type VII alpha 1 chain | Mõnikord (5–29%) | Esineb 2 haiguses |
| CTNNB1catenin beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DACT1dishevelled binding antagonist of beta catenin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DIAPH1diaphanous related formin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EIF5Aeukaryotic translation initiation factor 5A | Mõnikord (5–29%) | Esineb 1 haiguses |
| EXT2exostosin glycosyltransferase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FOXA2forkhead box A2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GHSRgrowth hormone secretagogue receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| GLI2GLI family zinc finger 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HBBhemoglobin subunit beta | Mõnikord (5–29%) | Esineb 2 haiguses |
| HDAC8histone deacetylase 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAU2MAU2 sister chromatid cohesion factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| MEN1menin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MMP1matrix metallopeptidase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ATP8mitochondrially encoded ATP synthase membrane subunit 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NDPnorrin cystine knot growth factor NDP | Mõnikord (5–29%) | Esineb 1 haiguses |
| NF1neurofibromin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NIPBLNIPBL cohesin loading factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| NLRP3NLR family pyrin domain containing 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NOTCH2notch receptor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Mõnikord (5–29%) | Esineb 1 haiguses |
| OTX2orthodenticle homeobox 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PCSK1proprotein convertase subtilisin/kexin type 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PGM1phosphoglucomutase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PHF21APHD finger protein 21A | Mõnikord (5–29%) | Esineb 1 haiguses |
| PHKA2phosphorylase kinase regulatory subunit alpha 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PHKG2phosphorylase kinase catalytic subunit gamma 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| POMCproopiomelanocortin | Mõnikord (5–29%) | Esineb 1 haiguses |
| PORcytochrome p450 oxidoreductase | Mõnikord (5–29%) | Esineb 1 haiguses |
| POU1F1POU class 1 homeobox 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PROP1PROP paired-like homeobox 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| PTRH2peptidyl-tRNA hydrolase 2 | Mõnikord (5–29%) | Esineb 2 haiguses |
| RAD21RAD21 cohesin complex component | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAI1retinoic acid induced 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RPL10ribosomal protein L10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Mõnikord (5–29%) | Esineb 1 haiguses |
| SALL1spalt like transcription factor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC12A3solute carrier family 12 member 3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| SLC37A4solute carrier family 37 member 4 | Mõnikord (5–29%) | Esineb 3 haiguses |
| SMC1Astructural maintenance of chromosomes 1A | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMC3structural maintenance of chromosomes 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SOX3SRY-box transcription factor 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| STAT3signal transducer and activator of transcription 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TGFB1transforming growth factor beta 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| TRIP4thyroid hormone receptor interactor 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| USP9Xubiquitin specific peptidase 9 X-linked | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZFXzinc finger protein X-linked | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZMPSTE24zinc metallopeptidase STE24 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPTBN1spectrin beta, non-erythrocytic 1 | Harva (1–4%) | Esineb 1 haiguses |
| ALDOAaldolase, fructose-bisphosphate A | Pole registreeritud | Esineb 1 haiguses |
| CENPTcentromere protein T | Pole registreeritud | Esineb 1 haiguses |
| CTNScystinosin, lysosomal cystine transporter | Pole registreeritud | Esineb 1 haiguses |
| CUL4Bcullin 4B | Pole registreeritud | Esineb 1 haiguses |
| EIF2S3eukaryotic translation initiation factor 2 subunit gamma | Pole registreeritud | Esineb 1 haiguses |
| FGD1FYVE, RhoGEF and PH domain containing 1 | Pole registreeritud | Esineb 1 haiguses |
| G6PC1glucose-6-phosphatase catalytic subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| GMNNgeminin DNA replication inhibitor | Pole registreeritud | Esineb 1 haiguses |
| HLA-DQA1major histocompatibility complex, class II, DQ alpha 1 | Pole registreeritud | Esineb 1 haiguses |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Pole registreeritud | Esineb 1 haiguses |
| LGR4leucine rich repeat containing G protein-coupled receptor 4 | Pole registreeritud | Esineb 1 haiguses |
| LHBluteinizing hormone subunit beta | Pole registreeritud | Esineb 1 haiguses |
| MSMO1methylsterol monooxygenase 1 | Pole registreeritud | Esineb 1 haiguses |
| PHF6PHD finger protein 6 | Pole registreeritud | Esineb 1 haiguses |
| PNPLA6patatin like domain 6, lysophospholipase | Pole registreeritud | Esineb 1 haiguses |
| POF1BPOF1B actin binding protein | Pole registreeritud | Esineb 1 haiguses |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Pole registreeritud | Esineb 1 haiguses |
| TCF12transcription factor 12 | Pole registreeritud | Esineb 1 haiguses |
| TGFB2transforming growth factor beta 2 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Kitsamad tunnused
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.16-c6eea6bf.
Üks test. Vastused kogu eluks.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast