Tunnus
Decreased activity of gonads
Kliiniline nimetus: Hypogonadism
A decreased functionality of the gonad.
Kokkuvõte
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Decreased activity of gonads, and the rest of your genome, with one test.
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Telli oma Genome Test171 geeni on seotud tunnusega Decreased activity of gonads
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Decreased activity of gonads. 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 |
|---|---|---|
| ALG1ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase | Alati | Esineb 1 haiguses |
| BBS12Bardet-Biedl syndrome 12 | Alati | Esineb 2 haiguses |
| BBS2Bardet-Biedl syndrome 2 | Alati | Esineb 2 haiguses |
| BBS5Bardet-Biedl syndrome 5 | Alati | Esineb 2 haiguses |
| BBS7Bardet-Biedl syndrome 7 | Alati | Esineb 2 haiguses |
| DCAF17DDB1 and CUL4 associated factor 17 | Alati | Esineb 2 haiguses |
| FANCBFA complementation group B | Alati | Esineb 2 haiguses |
| FEZF1FEZ family zinc finger 1 | Alati | Esineb 1 haiguses |
| HAMPhepcidin antimicrobial peptide | Alati | Esineb 2 haiguses |
| IFT74intraflagellar transport 74 | Alati | Esineb 2 haiguses |
| LZTFL1leucine zipper transcription factor like 1 | Alati | Esineb 2 haiguses |
| MDM2MDM2 proto-oncogene | Alati | Esineb 1 haiguses |
| PNPLA6patatin like domain 6, lysophospholipase | Alati | Esineb 3 haiguses |
| SLC30A7solute carrier family 30 member 7 | Alati | Esineb 1 haiguses |
| STEAP3STEAP3 metalloreductase | Alati | Esineb 2 haiguses |
| TP53tumor protein p53 | Alati | Esineb 1 haiguses |
| AIPAHR interacting HSP90 co-chaperone | Väga sageli (80–99%) | Esineb 1 haiguses |
| ALX4ALX homeobox 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ANK1ankyrin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CAMKMTcalmodulin-lysine N-methyltransferase | Väga sageli (80–99%) | Esineb 1 haiguses |
| CDH23cadherin related 23 | Väga sageli (80–99%) | Esineb 2 haiguses |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Väga sageli (80–99%) | Esineb 1 haiguses |
| DDB2damage specific DNA binding protein 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Väga sageli (80–99%) | Esineb 3 haiguses |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Väga sageli (80–99%) | Esineb 2 haiguses |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Väga sageli (80–99%) | Esineb 2 haiguses |
| ERCC5ERCC excision repair 5, endonuclease | Väga sageli (80–99%) | Esineb 2 haiguses |
| FMR1fragile X messenger ribonucleoprotein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LMNAlamin A/C | Väga sageli (80–99%) | Esineb 1 haiguses |
| MEN1menin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX1peroxisomal biogenesis factor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX6peroxisomal biogenesis factor 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PHF6PHD finger protein 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| POLEDNA polymerase epsilon, catalytic subunit | Väga sageli (80–99%) | Esineb 1 haiguses |
| PPM1Bprotein phosphatase, Mg2+/Mn2+ dependent 1B | Väga sageli (80–99%) | Esineb 1 haiguses |
| PREPLprolyl endopeptidase like | Väga sageli (80–99%) | Esineb 1 haiguses |
| RNF216ring finger protein 216 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SIL1SIL1 nucleotide exchange factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| SIM1SIM bHLH transcription factor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC3A1solute carrier family 3 member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
Näita veel 131 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TTC8tetratricopeptide repeat domain 8 | Väga sageli (80–99%) | Esineb 2 haiguses |
| WRNWRN RecQ like helicase | Väga sageli (80–99%) | Esineb 2 haiguses |
| XPAXPA, DNA damage recognition and repair factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| XPCXPC complex subunit, DNA damage recognition and repair factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZBTB20zinc finger and BTB domain containing 20 | Väga sageli (80–99%) | Esineb 1 haiguses |
| AIREautoimmune regulator | Sageli (30–79%) | Esineb 2 haiguses |
| ARL6ARF like GTPase 6 | Sageli (30–79%) | Esineb 2 haiguses |
| BBIP1BBSome interacting protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| BBS1Bardet-Biedl syndrome 1 | Sageli (30–79%) | Esineb 2 haiguses |
| BBS10Bardet-Biedl syndrome 10 | Sageli (30–79%) | Esineb 2 haiguses |
| BBS4Bardet-Biedl syndrome 4 | Sageli (30–79%) | Esineb 2 haiguses |
| BBS9Bardet-Biedl syndrome 9 | Sageli (30–79%) | Esineb 1 haiguses |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Sageli (30–79%) | Esineb 2 haiguses |
| CEP19centrosomal protein 19 | Sageli (30–79%) | Esineb 1 haiguses |
| CEP290centrosomal protein 290 | Sageli (30–79%) | Esineb 1 haiguses |
| CFAP418cilia and flagella associated protein 418 | Sageli (30–79%) | Esineb 1 haiguses |
| CHRNGcholinergic receptor nicotinic gamma subunit | Sageli (30–79%) | Esineb 1 haiguses |
| CTNNB1catenin beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Sageli (30–79%) | Esineb 1 haiguses |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Sageli (30–79%) | Esineb 1 haiguses |
| HJVhemojuvelin BMP co-receptor | Sageli (30–79%) | Esineb 1 haiguses |
| IFT172intraflagellar transport 172 | Sageli (30–79%) | Esineb 1 haiguses |
| IFT27intraflagellar transport 27 | Sageli (30–79%) | Esineb 2 haiguses |
| IGF1insulin like growth factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MAGEL2MAGE family member L2 | Sageli (30–79%) | Esineb 2 haiguses |
| MKKSMKKS centrosomal shuttling protein | Sageli (30–79%) | Esineb 1 haiguses |
| MKS1MKS transition zone complex subunit 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MYH3myosin heavy chain 3 | Sageli (30–79%) | Esineb 1 haiguses |
| NECTIN1nectin cell adhesion molecule 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NPHP1nephrocystin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SCAPERS-phase cyclin A associated protein in the ER | Sageli (30–79%) | Esineb 1 haiguses |
| SCLT1sodium channel and clathrin linker 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Sageli (30–79%) | Esineb 2 haiguses |
| SEMA3Asemaphorin 3A | Sageli (30–79%) | Esineb 1 haiguses |
| SOX10SRY-box transcription factor 10 | Sageli (30–79%) | Esineb 2 haiguses |
| TRIM32tripartite motif containing 32 | Sageli (30–79%) | Esineb 2 haiguses |
| USP7ubiquitin specific peptidase 7 | Sageli (30–79%) | Esineb 1 haiguses |
| WDPCPWD repeat containing planar cell polarity effector | Sageli (30–79%) | Esineb 1 haiguses |
| AMACRalpha-methylacyl-CoA racemase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ANAPC1anaphase promoting complex subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ANTXR1ANTXR cell adhesion molecule 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP5F1AATP synthase F1 subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP5F1DATP synthase F1 subunit delta | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP5F1EATP synthase F1 subunit epsilon | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP5MKATP synthase membrane subunit k | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP5POATP synthase peripheral stalk subunit OSCP | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATPAF2ATP synthase mitochondrial F1 complex assembly factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BCL11ABCL11 transcription factor A | Mõnikord (5–29%) | Esineb 1 haiguses |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRCA1BRCA1 DNA repair associated | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRCA2BRCA2 DNA repair associated | Mõnikord (5–29%) | Esineb 1 haiguses |
| BRIP1BRCA1 interacting DNA helicase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CASZ1castor zinc finger 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CISD2CDGSH iron sulfur domain 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CUL4Bcullin 4B | Mõnikord (5–29%) | Esineb 2 haiguses |
| FAAP100FA core complex associated protein 100 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCAFA complementation group A | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCCFA complementation group C | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCD2FA complementation group D2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCEFA complementation group E | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCFFA complementation group F | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCGFA complementation group G | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCIFA complementation group I | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCLFA complementation group L | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCMFA complementation group M | Mõnikord (5–29%) | Esineb 1 haiguses |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Mõnikord (5–29%) | Esineb 1 haiguses |
| HSPG2heparan sulfate proteoglycan 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IER3IP1immediate early response 3 interacting protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IFT54intraflagellar transport 54 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LUZP1leucine zipper protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAD2L2mitotic arrest deficient 2 like 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAP2K1mitogen-activated protein kinase kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MMP23Bmatrix metallopeptidase 23B | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ATP8mitochondrially encoded ATP synthase membrane subunit 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PALB2partner and localizer of BRCA2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PDE4Dphosphodiesterase 4D | Mõnikord (5–29%) | Esineb 1 haiguses |
| PDPNpodoplanin | Mõnikord (5–29%) | Esineb 1 haiguses |
| PHGDHphosphoglycerate dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRDM16PR/SET domain 16 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Mõnikord (5–29%) | Esineb 2 haiguses |
| PRKCZprotein kinase C zeta | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTDSS1phosphatidylserine synthase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAD51RAD51 recombinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAD51CRAD51 paralog C | Mõnikord (5–29%) | Esineb 1 haiguses |
| RELREL proto-oncogene, NF-kB subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| REREarginine-glutamic acid dipeptide repeats | Mõnikord (5–29%) | Esineb 1 haiguses |
| RFWD3ring finger and WD repeat domain 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SKISKI proto-oncogene | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC29A3solute carrier family 29 member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLX4SLX4 structure-specific endonuclease subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMAD4SMAD family member 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SNAP29synaptosome associated protein 29 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPENspen family transcriptional repressor | Mõnikord (5–29%) | Esineb 1 haiguses |
| STSsteroid sulfatase | Mõnikord (5–29%) | Esineb 1 haiguses |
| STUB1STIP1 homology and U-box containing protein 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| TGFB1transforming growth factor beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TWNKtwinkle mtDNA helicase | Mõnikord (5–29%) | Esineb 1 haiguses |
| UBE2Tubiquitin conjugating enzyme E2 T | Mõnikord (5–29%) | Esineb 1 haiguses |
| UBE4Bubiquitination factor E4B | Mõnikord (5–29%) | Esineb 1 haiguses |
| VPS4Avacuolar protein sorting 4 homolog A | Mõnikord (5–29%) | Esineb 1 haiguses |
| WFS1wolframin ER transmembrane glycoprotein | Mõnikord (5–29%) | Esineb 1 haiguses |
| XPO1exportin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| XRCC2X-ray repair cross complementing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DNM1Ldynamin 1L | Harva (1–4%) | Esineb 1 haiguses |
| HBBhemoglobin subunit beta | Harva (1–4%) | Esineb 1 haiguses |
| MYT1Lmyelin transcription factor 1 like | Harva (1–4%) | Esineb 1 haiguses |
| OPA1OPA1 mitochondrial dynamin like GTPase | Harva (1–4%) | Esineb 1 haiguses |
| PPIBpeptidylprolyl isomerase B | Harva (1–4%) | Esineb 1 haiguses |
| ABCD1ATP binding cassette subfamily D member 1 | Pole registreeritud | Esineb 1 haiguses |
| ARandrogen receptor | Pole registreeritud | Esineb 1 haiguses |
| ARSLarylsulfatase L | Pole registreeritud | Esineb 1 haiguses |
| ATRXATRX chromatin remodeler | Pole registreeritud | Esineb 1 haiguses |
| CCDC28Bcoiled-coil domain containing 28B | Pole registreeritud | Esineb 1 haiguses |
| CNBPCCHC-type zinc finger nucleic acid binding protein | Pole registreeritud | Esineb 1 haiguses |
| DMPKDM1 protein kinase | Pole registreeritud | Esineb 1 haiguses |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Pole registreeritud | Esineb 1 haiguses |
| FGF17fibroblast growth factor 17 | Pole registreeritud | Esineb 1 haiguses |
| FSHBfollicle stimulating hormone subunit beta | Pole registreeritud | Esineb 1 haiguses |
| GNASGNAS complex locus | Pole registreeritud | Esineb 2 haiguses |
| HDAC8histone deacetylase 8 | Pole registreeritud | Esineb 1 haiguses |
| IL17RDinterleukin 17 receptor D | Pole registreeritud | Esineb 1 haiguses |
| LEPleptin | Pole registreeritud | Esineb 1 haiguses |
| PROP1PROP paired-like homeobox 1 | Pole registreeritud | Esineb 1 haiguses |
| RECQL4RecQ like helicase 4 | Pole registreeritud | Esineb 1 haiguses |
| SGPL1sphingosine-1-phosphate lyase 1 | Pole registreeritud | Esineb 1 haiguses |
| SLC39A4solute carrier family 39 member 4 | 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