VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Dehydration, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test111 geeni on seotud tunnusega Dehydration
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Dehydration. 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 |
|---|---|---|
| AGXTalanine--glyoxylate aminotransferase | Alati | Esineb 1 haiguses |
| ATP6V1B1ATPase H+ transporting V1 subunit B1 | Alati | Esineb 1 haiguses |
| CLMPCXADR like cell adhesion molecule | Alati | Esineb 1 haiguses |
| CTNScystinosin, lysosomal cystine transporter | Alati | Esineb 3 haiguses |
| CYC1cytochrome c1 | Alati | Esineb 1 haiguses |
| DNM1Ldynamin 1L | Alati | Esineb 1 haiguses |
| EGFRepidermal growth factor receptor | Alati | Esineb 1 haiguses |
| MAN2B2mannosidase alpha class 2B member 2 | Alati | Esineb 1 haiguses |
| MCEEmethylmalonyl-CoA epimerase | Alati | Esineb 1 haiguses |
| MMADHCmetabolism of cobalamin associated D | Alati | Esineb 1 haiguses |
| MPV17mitochondrial inner membrane protein MPV17 | Alati | Esineb 1 haiguses |
| MRPS28mitochondrial ribosomal protein S28 | Alati | Esineb 1 haiguses |
| NEUROG3neurogenin 3 | Alati | Esineb 2 haiguses |
| NHEJ1non-homologous end joining factor 1 | Alati | Esineb 1 haiguses |
| SCNN1Asodium channel epithelial 1 subunit alpha | Alati | Esineb 2 haiguses |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Alati | Esineb 2 haiguses |
| SLC12A1solute carrier family 12 member 1 | Alati | Esineb 1 haiguses |
| SPINK5serine peptidase inhibitor Kazal type 5 | Alati | Esineb 1 haiguses |
| ABCC8ATP binding cassette subfamily C member 8 | Väga sageli (80–99%) | Esineb 3 haiguses |
| CYP11A1cytochrome P450 family 11 subfamily A member 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| GCKglucokinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| HYMAIhydatidiform mole associated and imprinted | Väga sageli (80–99%) | Esineb 3 haiguses |
| INSinsulin | Väga sageli (80–99%) | Esineb 1 haiguses |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Väga sageli (80–99%) | Esineb 3 haiguses |
| MMUTmethylmalonyl-CoA mutase | Väga sageli (80–99%) | Esineb 2 haiguses |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Väga sageli (80–99%) | Esineb 1 haiguses |
| PDX1pancreatic and duodenal homeobox 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PLAGL1PLAG1 like zinc finger 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| SLC5A1solute carrier family 5 member 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| STAT3signal transducer and activator of transcription 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZFP57ZFP57 zinc finger protein | Väga sageli (80–99%) | Esineb 2 haiguses |
| ACAT1acetyl-CoA acetyltransferase 1 | Sageli (30–79%) | Esineb 2 haiguses |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Sageli (30–79%) | Esineb 3 haiguses |
| EPCAMepithelial cell adhesion molecule | Sageli (30–79%) | Esineb 1 haiguses |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Sageli (30–79%) | Esineb 1 haiguses |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MYO5Bmyosin VB | Sageli (30–79%) | Esineb 2 haiguses |
| SCNN1Bsodium channel epithelial 1 subunit beta | Sageli (30–79%) | Esineb 2 haiguses |
| SLC22A5solute carrier family 22 member 5 | Sageli (30–79%) | Esineb 1 haiguses |
| STX3syntaxin 3 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 71 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| UNC45Aunc-45 myosin chaperone A | Sageli (30–79%) | Esineb 1 haiguses |
| ABCA12ATP binding cassette subfamily A member 12 | Mõnikord (5–29%) | Esineb 2 haiguses |
| ACAD8acyl-CoA dehydrogenase family member 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ACSF3acyl-CoA synthetase family member 3 | Mõnikord (5–29%) | Esineb 2 haiguses |
| AK2adenylate kinase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ASPRV1aspartic peptidase retroviral like 1 | Mõnikord (5–29%) | 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 |
| BLNKB cell linker | Mõnikord (5–29%) | Esineb 1 haiguses |
| BSNDbarttin CLCNK type accessory subunit beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Mõnikord (5–29%) | Esineb 1 haiguses |
| CD79ACD79a molecule | Mõnikord (5–29%) | Esineb 1 haiguses |
| CD79BCD79b molecule | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Mõnikord (5–29%) | Esineb 1 haiguses |
| CFTRCF transmembrane conductance regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| CLCNKAchloride voltage-gated channel Ka | Mõnikord (5–29%) | Esineb 1 haiguses |
| CLCNKBchloride voltage-gated channel Kb | Mõnikord (5–29%) | Esineb 2 haiguses |
| CLPBClpB family mitochondrial disaggregase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CYP4F22cytochrome P450 family 4 subfamily F member 22 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DBHdopamine beta-hydroxylase | Mõnikord (5–29%) | Esineb 1 haiguses |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FCGR2AFc gamma receptor IIa | Mõnikord (5–29%) | Esineb 1 haiguses |
| GATMglycine amidinotransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Mõnikord (5–29%) | Esineb 2 haiguses |
| IGHMimmunoglobulin heavy constant mu | Mõnikord (5–29%) | Esineb 1 haiguses |
| IGLL1immunoglobulin lambda like polypeptide 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LAMA3laminin subunit alpha 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LAMB3laminin subunit beta 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LAMC2laminin subunit gamma 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LIPNlipase family member N | Mõnikord (5–29%) | Esineb 1 haiguses |
| LRRC8Aleucine rich repeat containing 8 VRAC subunit A | Mõnikord (5–29%) | Esineb 1 haiguses |
| MEN1menin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MMACHCmetabolism of cobalamin associated C | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NARS2asparaginyl-tRNA synthetase 2, mitochondrial | Mõnikord (5–29%) | Esineb 1 haiguses |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NIPAL4NIPA like domain containing 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NLRP3NLR family pyrin domain containing 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| OXCT13-oxoacid CoA-transferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | 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 |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | 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 |
| SLC34A1solute carrier family 34 member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC5A2solute carrier family 5 member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPI1Spi-1 proto-oncogene | Mõnikord (5–29%) | Esineb 1 haiguses |
| SULT2B1sulfotransferase family 2B member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TCF3transcription factor 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TGFB1transforming growth factor beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TGM1transglutaminase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP6V0A4ATPase H+ transporting V0 subunit a4 | Pole registreeritud | Esineb 1 haiguses |
| CYP24A1cytochrome P450 family 24 subfamily A member 1 | Pole registreeritud | Esineb 1 haiguses |
| IVDisovaleryl-CoA dehydrogenase | Pole registreeritud | Esineb 1 haiguses |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Pole registreeritud | Esineb 1 haiguses |
| LCTlactase | Pole registreeritud | Esineb 1 haiguses |
| MMAAmetabolism of cobalamin associated A | Pole registreeritud | Esineb 1 haiguses |
| MMABmetabolism of cobalamin associated B | Pole registreeritud | Esineb 1 haiguses |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Pole registreeritud | Esineb 1 haiguses |
| NR3C2nuclear receptor subfamily 3 group C member 2 | Pole registreeritud | Esineb 1 haiguses |
| PCCApropionyl-CoA carboxylase subunit alpha | Pole registreeritud | Esineb 1 haiguses |
| PCCBpropionyl-CoA carboxylase subunit beta | Pole registreeritud | Esineb 1 haiguses |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Pole registreeritud | Esineb 1 haiguses |
| SLC26A3solute carrier family 26 member 3 | Pole registreeritud | Esineb 1 haiguses |
| VPS33BVPS33B late endosome and lysosome associated | 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