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Low blood potassium levels
Klinisk navn: Hypokalemia
The concentration of potassium(1+) in the blood circulation is below the lower limit of normal.
Resumé
- Også kaldet
- Decreased potassium(1+) concentration, Decreased potassium(1+) level, Decreased potassium(1+) level in blood, Reduced potassium(1+) concentration, Reduced potassium(1+) level, Reduced potassium(1+) level in blood
- Kropssystem
- Laboratory abnormality
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library(jsonlite)
url <- "https://dantelabs.com/traits/hypokalemia.json"
page <- fromJSON(url)
page$trait$nameLow blood potassium levelsHP:0002900
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Læs de gener, der er knyttet til Low blood potassium levels, og resten af dit genom, med én test.
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Bestil min Genome Test62 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Bartter DiseaseReads 5 of these genesBSNDCLCNKBKCNJ1SLC12A1MAGED2About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 8 of these genesCACNA1DSCNN1ASCNN1BSCNN1GCYP11B1HSD11B2About this report →
- Familial Periodic ParalysisReads 3 of these genesCACNA1SSCN4AKCNJ2About this report →
- Renal Tubular AcidosisReads 4 of these genesSLC4A4ATP6V0A4ATP6V1B1SLC4A1About this report →
Show 58 more reports
- Familial HypomagnesemiaReads 5 of these genesATP1A1KCNJ10FXYD2RRAGDCLDN10About this report →
- Juvenile Polyposis SyndromeReads 2 of these genesBMPR1ASMAD4About this report →
- Fanconi Renotubular Syndrome and Renal GlucosuriaReads 2 of these genesEHHADHGATMAbout this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- CystinosisReads 1 of these genesCTNSAbout this report →
- Gitelman SyndromeReads 1 of these genesSLC12A3About this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- Congenital Adrenal HyperplasiaReads 2 of these genesCYP11B1CYP17A1About this report →
- Dent Disease and Lowe SyndromeReads 1 of these genesOCRLAbout this report →
- Familial Isolated Pituitary Adenoma (FIPA / X-LAG)Reads 1 of these genesAIPAbout this report →
- Hereditary Mixed Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- Hypercalcemia InfantileReads 1 of these genesSLC34A1About this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesCACNA1SAbout this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesINSRAbout this report →
- Cerebral Creatine Deficiency SyndromesReads 1 of these genesGATMAbout this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Familial Atrial FibrillationReads 1 of these genesKCNJ2About this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- MelanomaReads 1 of these genesCDKN2AAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesPRKAR1AAbout this report →
- Short Qt SyndromeReads 1 of these genesKCNJ2About this report →
- Hereditary SpherocytosisReads 1 of these genesSLC4A1About this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 1 of these genesCASRAbout this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesTERTAbout this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesDEF6About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR3C1About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesTP53About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesCACNA1DAbout this report →
- Red Blood Cell Membrane DisordersReads 1 of these genesSLC4A1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesKCNJ10SCN4AAbout this report →
- Familial Pulmonary FibrosisReads 1 of these genesTERTAbout this report →
- Kidney CancerReads 1 of these genesTP53About this report →
- Long QT SyndromeReads 1 of these genesKCNJ2About this report →
- HyperinsulinismReads 1 of these genesINSRAbout this report →
- Polycystic Kidney DiseaseReads 1 of these genesPKD2About this report →
- Usher SyndromeReads 1 of these genesCDH23About this report →
- Urea Cycle DisorderReads 1 of these genesASLAbout this report →
- Urinary and Renal System TumourReads 1 of these genesTP53About this report →
- Congenital Diarrhoeas & EnteropathiesReads 1 of these genesSLC26A3About this report →
- Glycogen Storage DiseaseReads 1 of these genesSLC2A2About this report →
- Neonatal Diabetes MellitusReads 1 of these genesSLC2A2About this report →
- Dyskeratosis CongenitaReads 1 of these genesTERTAbout this report →
- Congenital Myasthenic SyndromeReads 1 of these genesSCN4AAbout this report →
- VitreoretinopathyReads 1 of these genesCTNNB1About this report →
- Diabetes MellitusReads 1 of these genesSLC2A2About this report →
- Thyroid CancerReads 1 of these genesCASRAbout this report →
- Severe Combined ImmunodeficiencyReads 1 of these genesNHEJ1About this report →
- Other Inborn Errors of ImmunityReads 2 of these genesNHEJ1DEF6About this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesATP1A1NDUFAF6About this report →
- Intellectual DisabilityReads 2 of these genesCTNNB1SMAD4About this report →
- Lysosomal Storage DiseaseReads 1 of these genesCTNSAbout this report →
- Leigh SyndromeReads 1 of these genesNDUFAF6About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesATP1A1About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesCLCN2About this report →
- Hearing Loss and DeafnessReads 1 of these genesCDH23About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesNDUFAF6About this report →
- Inherited Neurodegenerative DisordersReads 1 of these genesCLCN2About this report →
Læs de gener, der er knyttet til Low blood potassium levels, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test62 gener knyttet til Low blood potassium levels
Ændringer i disse gener forårsager sjældne tilstande, hvor Low blood potassium levels 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 |
|---|---|---|
| ATP1A1ATPase Na+/K+ transporting subunit alpha 1 | Altid | I 1 tilstand |
| BSNDbarttin CLCNK type accessory subunit beta | Altid | I 2 tilstande |
| CACNA1Dcalcium voltage-gated channel subunit alpha1 D | Altid | I 2 tilstande |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Altid | I 2 tilstande |
| CLCN2chloride voltage-gated channel 2 | Altid | I 2 tilstande |
| CLCNKBchloride voltage-gated channel Kb | Altid | I 4 tilstande |
| CTNScystinosin, lysosomal cystine transporter | Altid | I 3 tilstande |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Altid | I 1 tilstand |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Altid | I 2 tilstande |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Altid | I 1 tilstand |
| NHEJ1non-homologous end joining factor 1 | Altid | I 1 tilstand |
| PKD2polycystin 2, transient receptor potential cation channel | Altid | I 1 tilstand |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Altid | I 3 tilstande |
| SCNN1Asodium channel epithelial 1 subunit alpha | Altid | I 2 tilstande |
| SCNN1Bsodium channel epithelial 1 subunit beta | Altid | I 2 tilstande |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Altid | I 2 tilstande |
| SERPINA6serpin family A member 6 | Altid | I 1 tilstand |
| SLC12A1solute carrier family 12 member 1 | Altid | I 1 tilstand |
| SLC26A3solute carrier family 26 member 3 | Altid | I 1 tilstand |
| SLC4A4solute carrier family 4 member 4 | Altid | I 1 tilstand |
| ATP6V0A4ATPase H+ transporting V0 subunit a4 | Meget ofte (80–99 %) | I 1 tilstand |
| ATP6V1B1ATPase H+ transporting V1 subunit B1 | Meget ofte (80–99 %) | I 1 tilstand |
| CLCNKAchloride voltage-gated channel Ka | Meget ofte (80–99 %) | I 2 tilstande |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Meget ofte (80–99 %) | I 3 tilstande |
| HSD11B2hydroxysteroid 11-beta dehydrogenase 2 | Meget ofte (80–99 %) | I 2 tilstande |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Meget ofte (80–99 %) | I 2 tilstande |
| SLC12A3solute carrier family 12 member 3 | Meget ofte (80–99 %) | I 2 tilstande |
| CDKN2Acyclin dependent kinase inhibitor 2A | Ofte (30–79 %) | I 1 tilstand |
| CTNNB1catenin beta 1 | Ofte (30–79 %) | I 1 tilstand |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Ofte (30–79 %) | I 1 tilstand |
| DEF6DEF6 guanine nucleotide exchange factor | Ofte (30–79 %) | I 1 tilstand |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Ofte (30–79 %) | I 1 tilstand |
| FXYD2FXYD domain containing ion transport regulator 2 | Ofte (30–79 %) | I 1 tilstand |
| GATMglycine amidinotransferase | Ofte (30–79 %) | I 1 tilstand |
| GEMIN4gem nuclear organelle associated protein 4 | Ofte (30–79 %) | I 1 tilstand |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Ofte (30–79 %) | I 1 tilstand |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Ofte (30–79 %) | I 1 tilstand |
| NUP214nucleoporin 214 | Ofte (30–79 %) | I 1 tilstand |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Ofte (30–79 %) | I 1 tilstand |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Ofte (30–79 %) | I 1 tilstand |
Vis 22 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| RRAGDRas related GTP binding D | Ofte (30–79 %) | I 1 tilstand |
| SLC34A1solute carrier family 34 member 1 | Ofte (30–79 %) | I 1 tilstand |
| TERTtelomerase reverse transcriptase | Ofte (30–79 %) | I 1 tilstand |
| TP53tumor protein p53 | Ofte (30–79 %) | I 1 tilstand |
| ZNRF3zinc and ring finger 3 | Ofte (30–79 %) | I 1 tilstand |
| ASLargininosuccinate lyase | Nogle gange (5–29 %) | I 1 tilstand |
| CASRcalcium sensing receptor | Nogle gange (5–29 %) | I 1 tilstand |
| CDH23cadherin related 23 | Nogle gange (5–29 %) | I 1 tilstand |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| H6PDhexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase | Nogle gange (5–29 %) | I 1 tilstand |
| HSD11B1hydroxysteroid 11-beta dehydrogenase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| INSRinsulin receptor | Nogle gange (5–29 %) | I 2 tilstande |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Nogle gange (5–29 %) | I 2 tilstande |
| UNC45Aunc-45 myosin chaperone A | Nogle gange (5–29 %) | I 1 tilstand |
| AIPAHR interacting HSP90 co-chaperone | Ikke registreret | I 1 tilstand |
| BMPR1Abone morphogenetic protein receptor type 1A | Ikke registreret | I 1 tilstand |
| CLDN10claudin 10 | Ikke registreret | I 1 tilstand |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Ikke registreret | I 1 tilstand |
| MAGED2MAGE family member D2 | Ikke registreret | I 1 tilstand |
| SLC2A2solute carrier family 2 member 2 | Ikke registreret | I 1 tilstand |
| SMAD4SMAD family member 4 | Ikke registreret | I 1 tilstand |
| USP8ubiquitin specific peptidase 8 | 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.
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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 2026.10.21-777c9289.
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