Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Dehydration, and the rest of your genome, with one test.
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Get my Genome Test111 genes linked to Dehydration
Changes in these genes cause rare conditions in which Dehydration is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| AGXTalanine--glyoxylate aminotransferase | Always | In 1 condition |
| ATP6V1B1ATPase H+ transporting V1 subunit B1 | Always | In 1 condition |
| CLMPCXADR like cell adhesion molecule | Always | In 1 condition |
| CTNScystinosin, lysosomal cystine transporter | Always | In 3 conditions |
| CYC1cytochrome c1 | Always | In 1 condition |
| DNM1Ldynamin 1L | Always | In 1 condition |
| EGFRepidermal growth factor receptor | Always | In 1 condition |
| MAN2B2mannosidase alpha class 2B member 2 | Always | In 1 condition |
| MCEEmethylmalonyl-CoA epimerase | Always | In 1 condition |
| MMADHCmetabolism of cobalamin associated D | Always | In 1 condition |
| MPV17mitochondrial inner membrane protein MPV17 | Always | In 1 condition |
| MRPS28mitochondrial ribosomal protein S28 | Always | In 1 condition |
| NEUROG3neurogenin 3 | Always | In 2 conditions |
| NHEJ1non-homologous end joining factor 1 | Always | In 1 condition |
| SCNN1Asodium channel epithelial 1 subunit alpha | Always | In 2 conditions |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Always | In 2 conditions |
| SLC12A1solute carrier family 12 member 1 | Always | In 1 condition |
| SPINK5serine peptidase inhibitor Kazal type 5 | Always | In 1 condition |
| ABCC8ATP binding cassette subfamily C member 8 | Very often (80–99%) | In 3 conditions |
| CYP11A1cytochrome P450 family 11 subfamily A member 1 | Very often (80–99%) | In 2 conditions |
| GCKglucokinase | Very often (80–99%) | In 1 condition |
| HYMAIhydatidiform mole associated and imprinted | Very often (80–99%) | In 3 conditions |
| INSinsulin | Very often (80–99%) | In 1 condition |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Very often (80–99%) | In 3 conditions |
| MMUTmethylmalonyl-CoA mutase | Very often (80–99%) | In 2 conditions |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Very often (80–99%) | In 1 condition |
| PDX1pancreatic and duodenal homeobox 1 | Very often (80–99%) | In 1 condition |
| PLAGL1PLAG1 like zinc finger 1 | Very often (80–99%) | In 3 conditions |
| SLC5A1solute carrier family 5 member 1 | Very often (80–99%) | In 1 condition |
| STAT3signal transducer and activator of transcription 3 | Very often (80–99%) | In 1 condition |
| ZFP57ZFP57 zinc finger protein | Very often (80–99%) | In 2 conditions |
| ACAT1acetyl-CoA acetyltransferase 1 | Often (30–79%) | In 2 conditions |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Often (30–79%) | In 3 conditions |
| EPCAMepithelial cell adhesion molecule | Often (30–79%) | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Often (30–79%) | In 1 condition |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Often (30–79%) | In 1 condition |
| MYO5Bmyosin VB | Often (30–79%) | In 2 conditions |
| SCNN1Bsodium channel epithelial 1 subunit beta | Often (30–79%) | In 2 conditions |
| SLC22A5solute carrier family 22 member 5 | Often (30–79%) | In 1 condition |
| STX3syntaxin 3 | Often (30–79%) | In 1 condition |
Show 71 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| UNC45Aunc-45 myosin chaperone A | Often (30–79%) | In 1 condition |
| ABCA12ATP binding cassette subfamily A member 12 | Sometimes (5–29%) | In 2 conditions |
| ACAD8acyl-CoA dehydrogenase family member 8 | Sometimes (5–29%) | In 1 condition |
| ACSF3acyl-CoA synthetase family member 3 | Sometimes (5–29%) | In 2 conditions |
| AK2adenylate kinase 2 | Sometimes (5–29%) | In 1 condition |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Sometimes (5–29%) | In 1 condition |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Sometimes (5–29%) | In 1 condition |
| ASPRV1aspartic peptidase retroviral like 1 | Sometimes (5–29%) | In 1 condition |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Sometimes (5–29%) | In 1 condition |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Sometimes (5–29%) | In 1 condition |
| BLNKB cell linker | Sometimes (5–29%) | In 1 condition |
| BSNDbarttin CLCNK type accessory subunit beta | Sometimes (5–29%) | In 1 condition |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Sometimes (5–29%) | In 1 condition |
| CD79ACD79a molecule | Sometimes (5–29%) | In 1 condition |
| CD79BCD79b molecule | Sometimes (5–29%) | In 1 condition |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Sometimes (5–29%) | In 1 condition |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Sometimes (5–29%) | In 1 condition |
| CFTRCF transmembrane conductance regulator | Sometimes (5–29%) | In 1 condition |
| CLCNKAchloride voltage-gated channel Ka | Sometimes (5–29%) | In 1 condition |
| CLCNKBchloride voltage-gated channel Kb | Sometimes (5–29%) | In 2 conditions |
| CLPBClpB family mitochondrial disaggregase | Sometimes (5–29%) | In 1 condition |
| CYP4F22cytochrome P450 family 4 subfamily F member 22 | Sometimes (5–29%) | In 1 condition |
| DBHdopamine beta-hydroxylase | Sometimes (5–29%) | In 1 condition |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Sometimes (5–29%) | In 1 condition |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Sometimes (5–29%) | In 1 condition |
| FCGR2AFc gamma receptor IIa | Sometimes (5–29%) | In 1 condition |
| GATMglycine amidinotransferase | Sometimes (5–29%) | In 1 condition |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Sometimes (5–29%) | In 2 conditions |
| IGHMimmunoglobulin heavy constant mu | Sometimes (5–29%) | In 1 condition |
| IGLL1immunoglobulin lambda like polypeptide 1 | Sometimes (5–29%) | In 1 condition |
| LAMA3laminin subunit alpha 3 | Sometimes (5–29%) | In 1 condition |
| LAMB3laminin subunit beta 3 | Sometimes (5–29%) | In 1 condition |
| LAMC2laminin subunit gamma 2 | Sometimes (5–29%) | In 1 condition |
| LIPNlipase family member N | Sometimes (5–29%) | In 1 condition |
| LRRC8Aleucine rich repeat containing 8 VRAC subunit A | Sometimes (5–29%) | In 1 condition |
| MEN1menin 1 | Sometimes (5–29%) | In 1 condition |
| MMACHCmetabolism of cobalamin associated C | Sometimes (5–29%) | In 1 condition |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Sometimes (5–29%) | In 1 condition |
| NARS2asparaginyl-tRNA synthetase 2, mitochondrial | Sometimes (5–29%) | In 1 condition |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Sometimes (5–29%) | In 1 condition |
| NIPAL4NIPA like domain containing 4 | Sometimes (5–29%) | In 1 condition |
| NLRP3NLR family pyrin domain containing 3 | Sometimes (5–29%) | In 1 condition |
| OXCT13-oxoacid CoA-transferase 1 | Sometimes (5–29%) | In 1 condition |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Sometimes (5–29%) | In 1 condition |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sometimes (5–29%) | In 1 condition |
| RHOBTB2Rho related BTB domain containing 2 | Sometimes (5–29%) | In 1 condition |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Sometimes (5–29%) | In 1 condition |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Sometimes (5–29%) | In 1 condition |
| SLC1A3solute carrier family 1 member 3 | Sometimes (5–29%) | In 1 condition |
| SLC2A1solute carrier family 2 member 1 | Sometimes (5–29%) | In 1 condition |
| SLC34A1solute carrier family 34 member 1 | Sometimes (5–29%) | In 1 condition |
| SLC5A2solute carrier family 5 member 2 | Sometimes (5–29%) | In 1 condition |
| SPI1Spi-1 proto-oncogene | Sometimes (5–29%) | In 1 condition |
| SULT2B1sulfotransferase family 2B member 1 | Sometimes (5–29%) | In 1 condition |
| TCF3transcription factor 3 | Sometimes (5–29%) | In 1 condition |
| TGFB1transforming growth factor beta 1 | Sometimes (5–29%) | In 1 condition |
| TGM1transglutaminase 1 | Sometimes (5–29%) | In 1 condition |
| ATP6V0A4ATPase H+ transporting V0 subunit a4 | Not recorded | In 1 condition |
| CYP24A1cytochrome P450 family 24 subfamily A member 1 | Not recorded | In 1 condition |
| IVDisovaleryl-CoA dehydrogenase | Not recorded | In 1 condition |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Not recorded | In 1 condition |
| LCTlactase | Not recorded | In 1 condition |
| MMAAmetabolism of cobalamin associated A | Not recorded | In 1 condition |
| MMABmetabolism of cobalamin associated B | Not recorded | In 1 condition |
| NR0B1nuclear receptor subfamily 0 group B member 1 | Not recorded | In 1 condition |
| NR3C2nuclear receptor subfamily 3 group C member 2 | Not recorded | In 1 condition |
| PCCApropionyl-CoA carboxylase subunit alpha | Not recorded | In 1 condition |
| PCCBpropionyl-CoA carboxylase subunit beta | Not recorded | In 1 condition |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Not recorded | In 1 condition |
| SLC26A3solute carrier family 26 member 3 | Not recorded | In 1 condition |
| VPS33BVPS33B late endosome and lysosome associated | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
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Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
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