ReferencegenomGRCh38hg38
Positioner på gen- og variantsider følger dette valg i denne browser.
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Bestil min Genome Test111 gener knyttet til Dehydration
Ændringer i disse gener forårsager sjældne tilstande, hvor Dehydration ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| AGXTalanine--glyoxylate aminotransferase | Altid | I 1 tilstand |
| ATP6V1B1ATPase H+ transporting V1 subunit B1 | Altid | I 1 tilstand |
| CLMPCXADR like cell adhesion molecule | Altid | I 1 tilstand |
| CTNScystinosin, lysosomal cystine transporter | Altid | I 3 tilstande |
| CYC1cytochrome c1 | Altid | I 1 tilstand |
| DNM1Ldynamin 1L | Altid | I 1 tilstand |
| EGFRepidermal growth factor receptor | Altid | I 1 tilstand |
| MAN2B2mannosidase alpha class 2B member 2 | Altid | I 1 tilstand |
| MCEEmethylmalonyl-CoA epimerase | Altid | I 1 tilstand |
| MMADHCmetabolism of cobalamin associated D | Altid | I 1 tilstand |
| MPV17mitochondrial inner membrane protein MPV17 | Altid | I 1 tilstand |
| MRPS28mitochondrial ribosomal protein S28 | Altid | I 1 tilstand |
| NEUROG3neurogenin 3 | Altid | I 2 tilstande |
| NHEJ1non-homologous end joining factor 1 | Altid | I 1 tilstand |
| SCNN1Asodium channel epithelial 1 subunit alpha | Altid | I 2 tilstande |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Altid | I 2 tilstande |
| SLC12A1solute carrier family 12 member 1 | Altid | I 1 tilstand |
| SPINK5serine peptidase inhibitor Kazal type 5 | Altid | I 1 tilstand |
| ABCC8ATP binding cassette subfamily C member 8 | Meget ofte (80–99 %) | I 3 tilstande |
| CYP11A1cytochrome P450 family 11 subfamily A member 1 | Meget ofte (80–99 %) | I 2 tilstande |
| GCKglucokinase | Meget ofte (80–99 %) | I 1 tilstand |
| HYMAIhydatidiform mole associated and imprinted | Meget ofte (80–99 %) | I 3 tilstande |
| INSinsulin | Meget ofte (80–99 %) | I 1 tilstand |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Meget ofte (80–99 %) | I 3 tilstande |
| MMUTmethylmalonyl-CoA mutase | Meget ofte (80–99 %) | I 2 tilstande |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Meget ofte (80–99 %) | I 1 tilstand |
| PDX1pancreatic and duodenal homeobox 1 | Meget ofte (80–99 %) | I 1 tilstand |
| PLAGL1PLAG1 like zinc finger 1 | Meget ofte (80–99 %) | I 3 tilstande |
| SLC5A1solute carrier family 5 member 1 | Meget ofte (80–99 %) | I 1 tilstand |
| STAT3signal transducer and activator of transcription 3 | Meget ofte (80–99 %) | I 1 tilstand |
| ZFP57ZFP57 zinc finger protein | Meget ofte (80–99 %) | I 2 tilstande |
| ACAT1acetyl-CoA acetyltransferase 1 | Ofte (30–79 %) | I 2 tilstande |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Ofte (30–79 %) | I 3 tilstande |
| EPCAMepithelial cell adhesion molecule | Ofte (30–79 %) | I 1 tilstand |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Ofte (30–79 %) | I 1 tilstand |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Ofte (30–79 %) | I 1 tilstand |
| MYO5Bmyosin VB | Ofte (30–79 %) | I 2 tilstande |
| SCNN1Bsodium channel epithelial 1 subunit beta | Ofte (30–79 %) | I 2 tilstande |
| SLC22A5solute carrier family 22 member 5 | Ofte (30–79 %) | I 1 tilstand |
| STX3syntaxin 3 | Ofte (30–79 %) | I 1 tilstand |
Vis 71 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| UNC45Aunc-45 myosin chaperone A | Ofte (30–79 %) | I 1 tilstand |
| ABCA12ATP binding cassette subfamily A member 12 | Nogle gange (5–29 %) | I 2 tilstande |
| ACAD8acyl-CoA dehydrogenase family member 8 | Nogle gange (5–29 %) | I 1 tilstand |
| ACSF3acyl-CoA synthetase family member 3 | Nogle gange (5–29 %) | I 2 tilstande |
| AK2adenylate kinase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Nogle gange (5–29 %) | I 1 tilstand |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Nogle gange (5–29 %) | I 1 tilstand |
| ASPRV1aspartic peptidase retroviral like 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Nogle gange (5–29 %) | I 1 tilstand |
| BLNKB cell linker | Nogle gange (5–29 %) | I 1 tilstand |
| BSNDbarttin CLCNK type accessory subunit beta | Nogle gange (5–29 %) | I 1 tilstand |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Nogle gange (5–29 %) | I 1 tilstand |
| CD79ACD79a molecule | Nogle gange (5–29 %) | I 1 tilstand |
| CD79BCD79b molecule | Nogle gange (5–29 %) | I 1 tilstand |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Nogle gange (5–29 %) | I 1 tilstand |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Nogle gange (5–29 %) | I 1 tilstand |
| CFTRCF transmembrane conductance regulator | Nogle gange (5–29 %) | I 1 tilstand |
| CLCNKAchloride voltage-gated channel Ka | Nogle gange (5–29 %) | I 1 tilstand |
| CLCNKBchloride voltage-gated channel Kb | Nogle gange (5–29 %) | I 2 tilstande |
| CLPBClpB family mitochondrial disaggregase | Nogle gange (5–29 %) | I 1 tilstand |
| CYP4F22cytochrome P450 family 4 subfamily F member 22 | Nogle gange (5–29 %) | I 1 tilstand |
| DBHdopamine beta-hydroxylase | Nogle gange (5–29 %) | I 1 tilstand |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Nogle gange (5–29 %) | I 1 tilstand |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Nogle gange (5–29 %) | I 1 tilstand |
| FCGR2AFc gamma receptor IIa | Nogle gange (5–29 %) | I 1 tilstand |
| GATMglycine amidinotransferase | Nogle gange (5–29 %) | I 1 tilstand |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Nogle gange (5–29 %) | I 2 tilstande |
| IGHMimmunoglobulin heavy constant mu | Nogle gange (5–29 %) | I 1 tilstand |
| IGLL1immunoglobulin lambda like polypeptide 1 | Nogle gange (5–29 %) | I 1 tilstand |
| LAMA3laminin subunit alpha 3 | Nogle gange (5–29 %) | I 1 tilstand |
| LAMB3laminin subunit beta 3 | Nogle gange (5–29 %) | I 1 tilstand |
| LAMC2laminin subunit gamma 2 | Nogle gange (5–29 %) | I 1 tilstand |
| LIPNlipase family member N | Nogle gange (5–29 %) | I 1 tilstand |
| LRRC8Aleucine rich repeat containing 8 VRAC subunit A | Nogle gange (5–29 %) | I 1 tilstand |
| MEN1menin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MMACHCmetabolism of cobalamin associated C | Nogle gange (5–29 %) | I 1 tilstand |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Nogle gange (5–29 %) | I 1 tilstand |
| NARS2asparaginyl-tRNA synthetase 2, mitochondrial | Nogle gange (5–29 %) | I 1 tilstand |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Nogle gange (5–29 %) | I 1 tilstand |
| NIPAL4NIPA like domain containing 4 | Nogle gange (5–29 %) | I 1 tilstand |
| NLRP3NLR family pyrin domain containing 3 | Nogle gange (5–29 %) | I 1 tilstand |
| OXCT13-oxoacid CoA-transferase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Nogle gange (5–29 %) | I 1 tilstand |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RHOBTB2Rho related BTB domain containing 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC1A3solute carrier family 1 member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC2A1solute carrier family 2 member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC34A1solute carrier family 34 member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC5A2solute carrier family 5 member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SPI1Spi-1 proto-oncogene | Nogle gange (5–29 %) | I 1 tilstand |
| SULT2B1sulfotransferase family 2B member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TCF3transcription factor 3 | Nogle gange (5–29 %) | I 1 tilstand |
| TGFB1transforming growth factor beta 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TGM1transglutaminase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ATP6V0A4ATPase H+ transporting V0 subunit a4 | Ikke registreret | I 1 tilstand |
| CYP24A1cytochrome P450 family 24 subfamily A member 1 | Ikke registreret | I 1 tilstand |
| IVDisovaleryl-CoA dehydrogenase | Ikke registreret | I 1 tilstand |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Ikke registreret | I 1 tilstand |
| LCTlactase | Ikke registreret | I 1 tilstand |
| MMAAmetabolism of cobalamin associated A | Ikke registreret | I 1 tilstand |
| MMABmetabolism of cobalamin associated B | Ikke registreret | I 1 tilstand |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Ikke registreret | I 1 tilstand |
| NR3C2nuclear receptor subfamily 3 group C member 2 | Ikke registreret | I 1 tilstand |
| PCCApropionyl-CoA carboxylase subunit alpha | Ikke registreret | I 1 tilstand |
| PCCBpropionyl-CoA carboxylase subunit beta | Ikke registreret | I 1 tilstand |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Ikke registreret | I 1 tilstand |
| SLC26A3solute carrier family 26 member 3 | Ikke registreret | I 1 tilstand |
| VPS33BVPS33B late endosome and lysosome associated | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Snævrere træk
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.16-c6eea6bf.
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Fra 449 $Gratis forsendelse · Resultater på 6–8 uger