Tunnus
Excessive sweating
Kliiniline nimetus: Hyperhidrosis
Abnormal excessive perspiration (sweating) despite the lack of appropriate stimuli like hot and humid weather.
Kokkuvõte
- Teised nimetused
- Increased sweating, Profuse sweating, Sweating, Sweating profusely, Sweating, increased, Diaphoresis
- Kehasüsteem
- Abnormality of the integument
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Excessive sweating, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test137 geeni on seotud tunnusega Excessive sweating
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Excessive sweating. 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 |
|---|---|---|
| BOLA3bolA family member 3 | Alati | Esineb 1 haiguses |
| DSG1desmoglein 1 | Alati | Esineb 1 haiguses |
| IRF4interferon regulatory factor 4 | Alati | Esineb 1 haiguses |
| LIFRLIF receptor subunit alpha | Alati | Esineb 2 haiguses |
| MAP2K1mitogen-activated protein kinase kinase 1 | Alati | Esineb 2 haiguses |
| MAP2K2mitogen-activated protein kinase kinase 2 | Alati | Esineb 2 haiguses |
| SHQ1SHQ1, H/ACA ribonucleoprotein assembly factor | Alati | Esineb 1 haiguses |
| SLC18A2solute carrier family 18 member A2 | Alati | Esineb 2 haiguses |
| SUCLG1succinate-CoA ligase GDP/ADP-forming subunit alpha | Alati | Esineb 2 haiguses |
| AIPAHR interacting HSP90 co-chaperone | Väga sageli (80–99%) | Esineb 2 haiguses |
| AQP5aquaporin 5 | Väga sageli (80–99%) | Esineb 1 haiguses |
| BCL10BCL10 immune signaling adaptor | Väga sageli (80–99%) | Esineb 1 haiguses |
| BIRC3baculoviral IAP repeat containing 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Väga sageli (80–99%) | Esineb 2 haiguses |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Väga sageli (80–99%) | Esineb 1 haiguses |
| CLCF1cardiotrophin like cytokine factor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CRLF1cytokine receptor like factor 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ELP1elongator acetyltransferase complex subunit 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FOXP1forkhead box P1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FUCA1alpha-L-fucosidase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GABRA3gamma-aminobutyric acid type A receptor subunit alpha3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GPR101G protein-coupled receptor 101 | Väga sageli (80–99%) | Esineb 2 haiguses |
| HNF4Ahepatocyte nuclear factor 4 alpha | Väga sageli (80–99%) | Esineb 1 haiguses |
| HPGD15-hydroxyprostaglandin dehydrogenase | Väga sageli (80–99%) | Esineb 3 haiguses |
| IGHimmunoglobulin heavy locus | Väga sageli (80–99%) | Esineb 1 haiguses |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Väga sageli (80–99%) | Esineb 1 haiguses |
| KIF1Akinesin family member 1A | Väga sageli (80–99%) | Esineb 1 haiguses |
| KRASKRas proto-oncogene, GTPase | Väga sageli (80–99%) | Esineb 1 haiguses |
| MALT1MALT1 paracaspase | Väga sageli (80–99%) | Esineb 1 haiguses |
| MEN1menin 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| NLRP3NLR family pyrin domain containing 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PHOX2Bpaired like homeobox 2B | Väga sageli (80–99%) | Esineb 2 haiguses |
| RETREG1reticulophagy regulator 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SERPINB7serpin family B member 7 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLCO2A1solute carrier organic anion transporter family member 2A1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| WNK1WNK lysine deficient protein kinase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| YY1YY1 transcription factor | Väga sageli (80–99%) | Esineb 1 haiguses |
| ACDACD shelterin complex subunit and telomerase recruitment factor | Sageli (30–79%) | Esineb 1 haiguses |
| CDH23cadherin related 23 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 97 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| CDKN2Acyclin dependent kinase inhibitor 2A | Sageli (30–79%) | Esineb 1 haiguses |
| CLCN6Cl-/H+ antiporter 6 | Sageli (30–79%) | Esineb 1 haiguses |
| CTC1CST telomere replication complex component 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CTNNB1catenin beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CTSHcathepsin H | Sageli (30–79%) | Esineb 1 haiguses |
| DDCdopa decarboxylase | Sageli (30–79%) | Esineb 2 haiguses |
| DKC1dyskerin pseudouridine synthase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| DSTdystonin | Sageli (30–79%) | Esineb 1 haiguses |
| FGFR2fibroblast growth factor receptor 2 | Sageli (30–79%) | Esineb 2 haiguses |
| FLRT1fibronectin leucine rich transmembrane protein 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GNA14G protein subunit alpha 14 | Sageli (30–79%) | Esineb 2 haiguses |
| HCRThypocretin neuropeptide precursor | Sageli (30–79%) | Esineb 1 haiguses |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Sageli (30–79%) | Esineb 2 haiguses |
| JAK2Janus kinase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| JUPjunction plakoglobin | Sageli (30–79%) | Esineb 1 haiguses |
| KCNA1potassium voltage-gated channel subfamily A member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| KLC2kinesin light chain 2 | Sageli (30–79%) | Esineb 2 haiguses |
| MOGmyelin oligodendrocyte glycoprotein | Sageli (30–79%) | Esineb 1 haiguses |
| MPLMPL proto-oncogene, thrombopoietin receptor | Sageli (30–79%) | Esineb 1 haiguses |
| NGLY1N-glycanase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NHP2NHP2 ribonucleoprotein | Sageli (30–79%) | Esineb 1 haiguses |
| NOP10NOP10 ribonucleoprotein | Sageli (30–79%) | Esineb 1 haiguses |
| NPM1nucleophosmin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| P2RY11purinergic receptor P2Y11 | Sageli (30–79%) | Esineb 1 haiguses |
| PARNpoly(A)-specific ribonuclease | Sageli (30–79%) | Esineb 1 haiguses |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Sageli (30–79%) | Esineb 1 haiguses |
| PRNPprion protein (Kanno blood group) | Sageli (30–79%) | Esineb 2 haiguses |
| RTEL1regulator of telomere elongation helicase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC16A2solute carrier family 16 member 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SLURP1secreted LY6/PLAUR domain containing 1 | Sageli (30–79%) | Esineb 2 haiguses |
| SPRsepiapterin reductase | Sageli (30–79%) | Esineb 1 haiguses |
| SUCLA2succinate-CoA ligase ADP-forming subunit beta | Sageli (30–79%) | Esineb 1 haiguses |
| TATtyrosine aminotransferase | Sageli (30–79%) | Esineb 1 haiguses |
| TERCtelomerase RNA component | Sageli (30–79%) | Esineb 1 haiguses |
| TERTtelomerase reverse transcriptase | Sageli (30–79%) | Esineb 2 haiguses |
| THPOthrombopoietin | Sageli (30–79%) | Esineb 1 haiguses |
| TINF2TERF1 interacting nuclear factor 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TNFSF4TNF superfamily member 4 | Sageli (30–79%) | Esineb 1 haiguses |
| TP53tumor protein p53 | Sageli (30–79%) | Esineb 1 haiguses |
| TRANK1tetratricopeptide repeat and ankyrin repeat containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TYMSthymidylate synthetase | Sageli (30–79%) | Esineb 1 haiguses |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| WRAP53WD repeat containing antisense to TP53 | Sageli (30–79%) | Esineb 1 haiguses |
| ZNF365zinc finger protein 365 | Sageli (30–79%) | Esineb 1 haiguses |
| ZNRF3zinc and ring finger 3 | Sageli (30–79%) | Esineb 1 haiguses |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Mõnikord (5–29%) | Esineb 1 haiguses |
| CCND1cyclin D1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CNBPCCHC-type zinc finger nucleic acid binding protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| COL17A1collagen type XVII alpha 1 chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTSBcathepsin B | Mõnikord (5–29%) | Esineb 1 haiguses |
| CUL4Bcullin 4B | Mõnikord (5–29%) | Esineb 1 haiguses |
| FBXO11F-box protein 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GRB10growth factor receptor bound protein 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HLA-Bmajor histocompatibility complex, class I, B | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Mõnikord (5–29%) | Esineb 2 haiguses |
| KRT1keratin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRT14keratin 14 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRT16keratin 16 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRT5keratin 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRT9keratin 9 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PLAAphospholipase A2 activating protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RHOBTB2Rho related BTB domain containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC1A3solute carrier family 1 member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC2A1solute carrier family 2 member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC39A14solute carrier family 39 member 14 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPRED2sprouty related EVH1 domain containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRPV3transient receptor potential cation channel subfamily V member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| VHLvon Hippel-Lindau tumor suppressor | Mõnikord (5–29%) | Esineb 2 haiguses |
| WNT10AWnt family member 10A | Mõnikord (5–29%) | Esineb 1 haiguses |
| CLCNKBchloride voltage-gated channel Kb | Harva (1–4%) | Esineb 1 haiguses |
| GLAgalactosidase alpha | Harva (1–4%) | Esineb 1 haiguses |
| H19H19 imprinted maternally expressed transcript | Harva (1–4%) | Esineb 1 haiguses |
| HINT1histidine triad nucleotide binding protein 1 | Harva (1–4%) | Esineb 2 haiguses |
| HMBShydroxymethylbilane synthase | Harva (1–4%) | Esineb 1 haiguses |
| HRASHRas proto-oncogene, GTPase | Harva (1–4%) | Esineb 1 haiguses |
| IGF2insulin like growth factor 2 | Harva (1–4%) | Esineb 1 haiguses |
| NTRK1neurotrophic receptor tyrosine kinase 1 | Harva (1–4%) | Esineb 1 haiguses |
| SLC12A3solute carrier family 12 member 3 | Harva (1–4%) | Esineb 1 haiguses |
| COL6A1collagen type VI alpha 1 chain | Pole registreeritud | Esineb 1 haiguses |
| HEXBhexosaminidase subunit beta | Pole registreeritud | Esineb 1 haiguses |
| IGHMBP2immunoglobulin mu DNA binding protein 2 | Pole registreeritud | Esineb 1 haiguses |
| KIF1Bkinesin family member 1B | Pole registreeritud | Esineb 1 haiguses |
| KRT6Akeratin 6A | Pole registreeritud | Esineb 1 haiguses |
| MAXMYC associated transcriptional regulator X | Pole registreeritud | Esineb 1 haiguses |
| RETret proto-oncogene | Pole registreeritud | Esineb 1 haiguses |
| SCN11Asodium voltage-gated channel alpha subunit 11 | Pole registreeritud | Esineb 1 haiguses |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Pole registreeritud | Esineb 1 haiguses |
| SDHCsuccinate dehydrogenase complex subunit C | Pole registreeritud | Esineb 1 haiguses |
| SDHDsuccinate dehydrogenase complex subunit D | Pole registreeritud | Esineb 1 haiguses |
| TMEM127transmembrane protein 127 | 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