Tunnus
Absent sperm in semen
Kliiniline nimetus: Azoospermia
Absence of any measurable level of sperm,whereby spermatozoa cannot be observed even after centrifugation of the semen pellet.
Kokkuvõte
- Kehasüsteem
- Abnormality of the genitourinary system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Absent sperm in semen, and the rest of your genome, with one test.
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Telli oma Genome Test144 geeni on seotud tunnusega Absent sperm in semen
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Absent sperm in semen. 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 |
|---|---|---|
| C14orf39chromosome 14 open reading frame 39 | Alati | Esineb 1 haiguses |
| DCAF17DDB1 and CUL4 associated factor 17 | Alati | Esineb 1 haiguses |
| DNAH9dynein axonemal heavy chain 9 | Alati | Esineb 1 haiguses |
| LHBluteinizing hormone subunit beta | Alati | Esineb 1 haiguses |
| M1APmeiosis 1 associated protein | Alati | Esineb 1 haiguses |
| SCP2sterol carrier protein 2 | Alati | Esineb 1 haiguses |
| SLC29A3solute carrier family 29 member 3 | Alati | Esineb 2 haiguses |
| SOX9SRY-box transcription factor 9 | Alati | Esineb 2 haiguses |
| STEAP3STEAP3 metalloreductase | Alati | Esineb 2 haiguses |
| SYCP3synaptonemal complex protein 3 | Alati | Esineb 2 haiguses |
| TEX11testis expressed 11 | Alati | Esineb 2 haiguses |
| TEX14testis expressed 14, intercellular bridge forming factor | Alati | Esineb 2 haiguses |
| XRCC2X-ray repair cross complementing 2 | Alati | Esineb 3 haiguses |
| ZMYND15zinc finger MYND-type containing 15 | Alati | Esineb 2 haiguses |
| CATIPciliogenesis associated TTC17 interacting protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| CATSPER2cation channel sperm associated 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CCDC34coiled-coil domain containing 34 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CFTRCF transmembrane conductance regulator | Väga sageli (80–99%) | Esineb 2 haiguses |
| CHD7chromodomain helicase DNA binding protein 7 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CT55cancer/testis antigen 55 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DHX37DEAH-box helicase 37 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DNAH10dynein axonemal heavy chain 10 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DNHD1dynein heavy chain domain 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DUSP6dual specificity phosphatase 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| EMX2empty spiracles homeobox 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FANCMFA complementation group M | Väga sageli (80–99%) | Esineb 2 haiguses |
| FBXO43F-box protein 43 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FGF17fibroblast growth factor 17 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FGF8fibroblast growth factor 8 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FGFR1fibroblast growth factor receptor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GATA4GATA binding protein 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GCNAgerm cell nuclear acidic peptidase | Väga sageli (80–99%) | Esineb 2 haiguses |
| GNRH1gonadotropin releasing hormone 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GNRHRgonadotropin releasing hormone receptor | Väga sageli (80–99%) | Esineb 1 haiguses |
| HNF1BHNF1 homeobox B | Väga sageli (80–99%) | Esineb 1 haiguses |
| HS6ST1heparan sulfate 6-O-sulfotransferase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KISS1KiSS-1 metastasis suppressor | Väga sageli (80–99%) | Esineb 1 haiguses |
| KISS1RKISS1 receptor | Väga sageli (80–99%) | Esineb 2 haiguses |
| KLHL10kelch like family member 10 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
Näita veel 104 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| MEIOBmeiosis specific with OB-fold | Väga sageli (80–99%) | Esineb 1 haiguses |
| MOV10L1Mov10 like RNA helicase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MSH5mutS homolog 5 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NANOS1nanos C2HC-type zinc finger 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| NHLH2nescient helix-loop-helix 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| NSMFNMDA receptor synaptonuclear signaling and neuronal migration factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| PDHA2pyruvate dehydrogenase E1 subunit alpha 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PNLDC1PARN like ribonuclease domain containing exonuclease 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PROK2prokineticin 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PROKR2prokineticin receptor 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RBBP7RB binding protein 7, chromatin remodeling factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| RNF212ring finger protein 212 | Väga sageli (80–99%) | Esineb 1 haiguses |
| RPL10Lribosomal protein L10 like | Väga sageli (80–99%) | Esineb 1 haiguses |
| SHOC1shortage in chiasmata 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SOHLH1spermatogenesis and oogenesis specific basic helix-loop-helix 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SPAG17sperm associated antigen 17 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SPINK2serine peptidase inhibitor Kazal type 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SPRY4sprouty RTK signaling antagonist 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SRYsex determining region Y | Väga sageli (80–99%) | Esineb 3 haiguses |
| STAG3STAG3 cohesin complex component | Väga sageli (80–99%) | Esineb 1 haiguses |
| STRCstereocilin | Väga sageli (80–99%) | Esineb 1 haiguses |
| SYCE1synaptonemal complex central element protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TAC3tachykinin precursor 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TACR3tachykinin receptor 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TAF4BTATA-box binding protein associated factor 4b | Väga sageli (80–99%) | Esineb 2 haiguses |
| TDRD9tudor domain containing 9 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TERB1telomere repeat binding bouquet formation protein 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TERB2telomere repeat binding bouquet formation protein 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TEX15testis expressed 15, meiosis and synapsis associated | Väga sageli (80–99%) | Esineb 1 haiguses |
| VAMP7vesicle associated membrane protein 7 | Väga sageli (80–99%) | Esineb 1 haiguses |
| WDR11WD repeat domain 11 | Väga sageli (80–99%) | Esineb 1 haiguses |
| WNT4Wnt family member 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| WT1WT1 transcription factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| WWOXWW domain containing oxidoreductase | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZFPM2zinc finger protein, FOG family member 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZSWIM7zinc finger SWIM-type containing 7 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ANK1ankyrin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| BRCC3BRCA1/BRCA2-containing complex subunit 3 | Sageli (30–79%) | Esineb 1 haiguses |
| FSHBfollicle stimulating hormone subunit beta | Sageli (30–79%) | Esineb 2 haiguses |
| ARandrogen receptor | Mõnikord (5–29%) | Esineb 2 haiguses |
| BLMBLM RecQ like helicase | Mõnikord (5–29%) | Esineb 2 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 |
| CFAP57cilia and flagella associated protein 57 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| FAAP100FA core complex associated protein 100 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCAFA complementation group A | Mõnikord (5–29%) | Esineb 1 haiguses |
| FANCBFA complementation group B | 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 |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Mõnikord (5–29%) | Esineb 1 haiguses |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAD2L2mitotic arrest deficient 2 like 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Mõnikord (5–29%) | Esineb 1 haiguses |
| PALB2partner and localizer of BRCA2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAD51RAD51 recombinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| RAD51CRAD51 paralog C | Mõnikord (5–29%) | Esineb 1 haiguses |
| RFWD3ring finger and WD repeat domain 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLX4SLX4 structure-specific endonuclease subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| UBE2Tubiquitin conjugating enzyme E2 T | Mõnikord (5–29%) | Esineb 1 haiguses |
| GBA1glucosylceramidase beta 1 | Harva (1–4%) | Esineb 1 haiguses |
| MC2Rmelanocortin 2 receptor | Harva (1–4%) | Esineb 1 haiguses |
| MRAPmelanocortin 2 receptor accessory protein | Harva (1–4%) | Esineb 1 haiguses |
| NNTnicotinamide nucleotide transhydrogenase | Harva (1–4%) | Esineb 1 haiguses |
| STARsteroidogenic acute regulatory protein | Harva (1–4%) | Esineb 1 haiguses |
| TXNRD2thioredoxin reductase 2 | Harva (1–4%) | Esineb 1 haiguses |
| ADGRG2adhesion G protein-coupled receptor G2 | Pole registreeritud | Esineb 1 haiguses |
| ANOS1anosmin 1 | Pole registreeritud | Esineb 1 haiguses |
| BCL10BCL10 immune signaling adaptor | Pole registreeritud | Esineb 1 haiguses |
| BMP2bone morphogenetic protein 2 | Pole registreeritud | Esineb 1 haiguses |
| BPY2basic charge Y-linked 2 | Pole registreeritud | Esineb 1 haiguses |
| CDY1chromodomain Y-linked 1 | Pole registreeritud | Esineb 1 haiguses |
| CDY2Achromodomain Y-linked 2A | Pole registreeritud | Esineb 1 haiguses |
| CEP19centrosomal protein 19 | Pole registreeritud | Esineb 1 haiguses |
| CFAP221cilia and flagella associated protein 221 | Pole registreeritud | Esineb 1 haiguses |
| DAZ1deleted in azoospermia 1 | Pole registreeritud | Esineb 1 haiguses |
| DAZ2deleted in azoospermia 2 | Pole registreeritud | Esineb 1 haiguses |
| DAZ3deleted in azoospermia 3 | Pole registreeritud | Esineb 1 haiguses |
| DDX3YDEAD-box helicase 3 Y-linked | Pole registreeritud | Esineb 1 haiguses |
| FGFR3fibroblast growth factor receptor 3 | Pole registreeritud | Esineb 1 haiguses |
| HFEhomeostatic iron regulator | Pole registreeritud | Esineb 1 haiguses |
| HJVhemojuvelin BMP co-receptor | Pole registreeritud | Esineb 1 haiguses |
| HSFY1heat shock transcription factor Y-linked 1 | Pole registreeritud | Esineb 1 haiguses |
| KDM5Dlysine demethylase 5D | Pole registreeritud | Esineb 1 haiguses |
| KITKIT proto-oncogene, receptor tyrosine kinase | Pole registreeritud | Esineb 1 haiguses |
| MCM8minichromosome maintenance 8 homologous recombination repair factor | Pole registreeritud | Esineb 1 haiguses |
| MSH4mutS homolog 4 | Pole registreeritud | Esineb 1 haiguses |
| PRYPTPN13 like Y-linked | Pole registreeritud | Esineb 1 haiguses |
| PRY2PTPN13 like Y-linked 2 | Pole registreeritud | Esineb 1 haiguses |
| RBMY1A1RNA binding motif protein Y-linked family 1 member A1 | Pole registreeritud | Esineb 1 haiguses |
| RPS4Y2ribosomal protein S4 Y-linked 2 | Pole registreeritud | Esineb 1 haiguses |
| SEMA3Asemaphorin 3A | Pole registreeritud | Esineb 1 haiguses |
| STK11serine/threonine kinase 11 | Pole registreeritud | Esineb 1 haiguses |
| USP9Yubiquitin specific peptidase 9 Y-linked | Pole registreeritud | Esineb 1 haiguses |
| VCYvariable charge Y-linked | Pole registreeritud | Esineb 1 haiguses |
| XKRYXK related, Y-linked (pseudogene) | 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.
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Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast