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Tunnus
Enlarged male breast
Kliiniline nimetus: Gynecomastia
Abnormal development of large mammary glands in males resulting in breast enlargement.
Kokkuvõte
- Teised nimetused
- Gynaecomastia
- Kehasüsteem
- Abnormality of the breast
Enlarged male breastHP:0000771
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Read the genes linked to Enlarged male breast, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test99 geeni on seotud tunnusega Enlarged male breast
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Enlarged male breast. 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 |
|---|---|---|
| PLAAT3phospholipase A and acyltransferase 3 | Alati | Esineb 1 haiguses |
| RFC4replication factor C subunit 4 | Alati | Esineb 1 haiguses |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Alati | Esineb 1 haiguses |
| AKT2AKT serine/threonine kinase 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ARandrogen receptor | Väga sageli (80–99%) | Esineb 5 haiguses |
| CYP11A1cytochrome P450 family 11 subfamily A member 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| CYP19A1cytochrome P450 family 19 subfamily A member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| DHX37DEAH-box helicase 37 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GATA4GATA binding protein 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| HDAC8histone deacetylase 8 | Väga sageli (80–99%) | Esineb 1 haiguses |
| LAS1LLAS1 like ribosome biogenesis factor | Väga sageli (80–99%) | Esineb 2 haiguses |
| LEPleptin | Väga sageli (80–99%) | Esineb 2 haiguses |
| LEPRleptin receptor | Väga sageli (80–99%) | Esineb 1 haiguses |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PHF6PHD finger protein 6 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PNPLA6patatin like domain 6, lysophospholipase | Väga sageli (80–99%) | Esineb 1 haiguses |
| RBM28RNA binding motif protein 28 | Väga sageli (80–99%) | Esineb 2 haiguses |
| RNF216ring finger protein 216 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SOX9SRY-box transcription factor 9 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SRYsex determining region Y | Väga sageli (80–99%) | Esineb 3 haiguses |
| VAMP7vesicle associated membrane protein 7 | 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 |
| AIPAHR interacting HSP90 co-chaperone | Sageli (30–79%) | Esineb 1 haiguses |
| CDH23cadherin related 23 | Sageli (30–79%) | Esineb 2 haiguses |
| CHD7chromodomain helicase DNA binding protein 7 | Sageli (30–79%) | Esineb 2 haiguses |
| CPEcarboxypeptidase E | Sageli (30–79%) | Esineb 1 haiguses |
| CUL4Bcullin 4B | Sageli (30–79%) | Esineb 1 haiguses |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Sageli (30–79%) | Esineb 3 haiguses |
| DESdesmin | Sageli (30–79%) | Esineb 1 haiguses |
| DUSP6dual specificity phosphatase 6 | Sageli (30–79%) | Esineb 2 haiguses |
| EMX2empty spiracles homeobox 2 | Sageli (30–79%) | Esineb 2 haiguses |
| FGF17fibroblast growth factor 17 | Sageli (30–79%) | Esineb 2 haiguses |
| FGF8fibroblast growth factor 8 | Sageli (30–79%) | Esineb 2 haiguses |
| FGFR1fibroblast growth factor receptor 1 | Sageli (30–79%) | Esineb 3 haiguses |
| FMR1fragile X messenger ribonucleoprotein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GNRH1gonadotropin releasing hormone 1 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 59 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| GNRHRgonadotropin releasing hormone receptor | Sageli (30–79%) | Esineb 1 haiguses |
| HS6ST1heparan sulfate 6-O-sulfotransferase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| KISS1KiSS-1 metastasis suppressor | Sageli (30–79%) | Esineb 1 haiguses |
| KISS1RKISS1 receptor | Sageli (30–79%) | Esineb 2 haiguses |
| LHBluteinizing hormone subunit beta | Sageli (30–79%) | Esineb 1 haiguses |
| MEN1menin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NHLH2nescient helix-loop-helix 2 | Sageli (30–79%) | Esineb 1 haiguses |
| NSMFNMDA receptor synaptonuclear signaling and neuronal migration factor | Sageli (30–79%) | Esineb 2 haiguses |
| PROK2prokineticin 2 | Sageli (30–79%) | Esineb 2 haiguses |
| PROKR2prokineticin receptor 2 | Sageli (30–79%) | Esineb 2 haiguses |
| SLC29A3solute carrier family 29 member 3 | Sageli (30–79%) | Esineb 2 haiguses |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SPRY4sprouty RTK signaling antagonist 4 | Sageli (30–79%) | Esineb 2 haiguses |
| TAC3tachykinin precursor 3 | Sageli (30–79%) | Esineb 1 haiguses |
| TACR3tachykinin receptor 3 | Sageli (30–79%) | Esineb 2 haiguses |
| TCF20transcription factor 20 | Sageli (30–79%) | Esineb 1 haiguses |
| TTI1TELO2 interacting protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| WDR11WD repeat domain 11 | Sageli (30–79%) | Esineb 2 haiguses |
| ZBTB20zinc finger and BTB domain containing 20 | Sageli (30–79%) | Esineb 2 haiguses |
| AFF4ALF transcription elongation factor 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALMS1ALMS1 centrosome and basal body associated protein | Mõnikord (5–29%) | Esineb 2 haiguses |
| ANOS1anosmin 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| BCL11ABCL11 transcription factor A | Mõnikord (5–29%) | Esineb 1 haiguses |
| BMP6bone morphogenetic protein 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CCDC141coiled-coil domain containing 141 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CYB5Acytochrome b5 type A | Mõnikord (5–29%) | Esineb 1 haiguses |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DCCDCC netrin 1 receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| ERMARDER membrane associated RNA degradation | Mõnikord (5–29%) | Esineb 1 haiguses |
| FEZF1FEZ family zinc finger 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FLRT3fibronectin leucine rich transmembrane protein 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HESX1HESX homeobox 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HFEhomeostatic iron regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| HPGD15-hydroxyprostaglandin dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| HSD17B3hydroxysteroid 17-beta dehydrogenase 3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| IL17RDinterleukin 17 receptor D | Mõnikord (5–29%) | Esineb 1 haiguses |
| MECP2methyl-CpG binding protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NDNFneuron derived neurotrophic factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| PDE11Aphosphodiesterase 11A | Mõnikord (5–29%) | Esineb 1 haiguses |
| POLR3ARNA polymerase III subunit A | Mõnikord (5–29%) | Esineb 2 haiguses |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| PSMB8proteasome 20S subunit beta 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTENphosphatase and tensin homolog | Mõnikord (5–29%) | Esineb 2 haiguses |
| RELREL proto-oncogene, NF-kB subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| SEMA3Asemaphorin 3A | Mõnikord (5–29%) | Esineb 1 haiguses |
| SH3PXD2BSH3 and PX domains 2B | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMC5structural maintenance of chromosomes 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SOX10SRY-box transcription factor 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TMEM53transmembrane protein 53 | Mõnikord (5–29%) | Esineb 1 haiguses |
| XPO1exportin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COQ8Acoenzyme Q8A | Harva (1–4%) | Esineb 1 haiguses |
| SPTBN1spectrin beta, non-erythrocytic 1 | Harva (1–4%) | Esineb 1 haiguses |
| CYP21A2cytochrome P450 family 21 subfamily A member 2 | Pole registreeritud | Esineb 1 haiguses |
| ITGA3integrin subunit alpha 3 | Pole registreeritud | Esineb 1 haiguses |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Pole registreeritud | Esineb 1 haiguses |
| RSPO1R-spondin 1 | Pole registreeritud | Esineb 1 haiguses |
| STK11serine/threonine kinase 11 | 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.
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