Tratto
Low blood potassium levels
Nome clinico: Hypokalemia
The concentration of potassium(1+) in the blood circulation is below the lower limit of normal.
Riepilogo
- Detto anche
- 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
- Sistema corporeo
- Laboratory abnormality
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page$trait$nameLeggi i geni collegati a Low blood potassium levels e il resto del tuo genoma con un unico test.
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Ottieni il mio 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 →
Leggi i geni collegati a Low blood potassium levels e il resto del tuo genoma con un unico test.
A partire da 449 $Spedizione gratuita · Risultati in 6–8 settimane
Ottieni il mio Genome Test62 geni collegati a Low blood potassium levels
Alterazioni in questi geni causano malattie rare in cui si osserva Low blood potassium levels. La maggior parte delle persone con questo tratto non presenta nessuna di tali condizioni, e un gene di questo elenco non dice nulla sul genoma di nessuno in particolare.
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| ATP1A1ATPase Na+/K+ transporting subunit alpha 1 | Sempre | In 1 condizione |
| BSNDbarttin CLCNK type accessory subunit beta | Sempre | In 2 condizioni |
| CACNA1Dcalcium voltage-gated channel subunit alpha1 D | Sempre | In 2 condizioni |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Sempre | In 2 condizioni |
| CLCN2chloride voltage-gated channel 2 | Sempre | In 2 condizioni |
| CLCNKBchloride voltage-gated channel Kb | Sempre | In 4 condizioni |
| CTNScystinosin, lysosomal cystine transporter | Sempre | In 3 condizioni |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Sempre | In 1 condizione |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Sempre | In 2 condizioni |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Sempre | In 1 condizione |
| NHEJ1non-homologous end joining factor 1 | Sempre | In 1 condizione |
| PKD2polycystin 2, transient receptor potential cation channel | Sempre | In 1 condizione |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Sempre | In 3 condizioni |
| SCNN1Asodium channel epithelial 1 subunit alpha | Sempre | In 2 condizioni |
| SCNN1Bsodium channel epithelial 1 subunit beta | Sempre | In 2 condizioni |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Sempre | In 2 condizioni |
| SERPINA6serpin family A member 6 | Sempre | In 1 condizione |
| SLC12A1solute carrier family 12 member 1 | Sempre | In 1 condizione |
| SLC26A3solute carrier family 26 member 3 | Sempre | In 1 condizione |
| SLC4A4solute carrier family 4 member 4 | Sempre | In 1 condizione |
| ATP6V0A4ATPase H+ transporting V0 subunit a4 | Molto spesso (80–99%) | In 1 condizione |
| ATP6V1B1ATPase H+ transporting V1 subunit B1 | Molto spesso (80–99%) | In 1 condizione |
| CLCNKAchloride voltage-gated channel Ka | Molto spesso (80–99%) | In 2 condizioni |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Molto spesso (80–99%) | In 3 condizioni |
| HSD11B2hydroxysteroid 11-beta dehydrogenase 2 | Molto spesso (80–99%) | In 2 condizioni |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Molto spesso (80–99%) | In 2 condizioni |
| SLC12A3solute carrier family 12 member 3 | Molto spesso (80–99%) | In 2 condizioni |
| CDKN2Acyclin dependent kinase inhibitor 2A | Spesso (30–79%) | In 1 condizione |
| CTNNB1catenin beta 1 | Spesso (30–79%) | In 1 condizione |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Spesso (30–79%) | In 1 condizione |
| DEF6DEF6 guanine nucleotide exchange factor | Spesso (30–79%) | In 1 condizione |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Spesso (30–79%) | In 1 condizione |
| FXYD2FXYD domain containing ion transport regulator 2 | Spesso (30–79%) | In 1 condizione |
| GATMglycine amidinotransferase | Spesso (30–79%) | In 1 condizione |
| GEMIN4gem nuclear organelle associated protein 4 | Spesso (30–79%) | In 1 condizione |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Spesso (30–79%) | In 1 condizione |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Spesso (30–79%) | In 1 condizione |
| NUP214nucleoporin 214 | Spesso (30–79%) | In 1 condizione |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Spesso (30–79%) | In 1 condizione |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Spesso (30–79%) | In 1 condizione |
Mostra altri 22 geni
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| RRAGDRas related GTP binding D | Spesso (30–79%) | In 1 condizione |
| SLC34A1solute carrier family 34 member 1 | Spesso (30–79%) | In 1 condizione |
| TERTtelomerase reverse transcriptase | Spesso (30–79%) | In 1 condizione |
| TP53tumor protein p53 | Spesso (30–79%) | In 1 condizione |
| ZNRF3zinc and ring finger 3 | Spesso (30–79%) | In 1 condizione |
| ASLargininosuccinate lyase | A volte (5–29%) | In 1 condizione |
| CASRcalcium sensing receptor | A volte (5–29%) | In 1 condizione |
| CDH23cadherin related 23 | A volte (5–29%) | In 1 condizione |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | A volte (5–29%) | In 1 condizione |
| H6PDhexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase | A volte (5–29%) | In 1 condizione |
| HSD11B1hydroxysteroid 11-beta dehydrogenase 1 | A volte (5–29%) | In 1 condizione |
| INSRinsulin receptor | A volte (5–29%) | In 2 condizioni |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | A volte (5–29%) | In 2 condizioni |
| UNC45Aunc-45 myosin chaperone A | A volte (5–29%) | In 1 condizione |
| AIPAHR interacting HSP90 co-chaperone | Non registrato | In 1 condizione |
| BMPR1Abone morphogenetic protein receptor type 1A | Non registrato | In 1 condizione |
| CLDN10claudin 10 | Non registrato | In 1 condizione |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Non registrato | In 1 condizione |
| MAGED2MAGE family member D2 | Non registrato | In 1 condizione |
| SLC2A2solute carrier family 2 member 2 | Non registrato | In 1 condizione |
| SMAD4SMAD family member 4 | Non registrato | In 1 condizione |
| USP8ubiquitin specific peptidase 8 | Non registrato | In 1 condizione |
Con quale frequenza questo tratto si presenta tra le persone con una delle condizioni legate al gene, nella misura più alta riscontrata tra queste, secondo quanto registrato dall'Human Phenotype Ontology. Queste pagine descrivono tratti e la ricerca che li riguarda; non costituiscono una diagnosi, e per i sintomi il medico o il consulente genetico è la persona a cui rivolgersi.
Tratti più specifici
Tratti più generali
Fonte dei dati
- Human Phenotype Ontology, versione 2026-09-01: il tratto, i suoi nomi, la sua definizione e i geni a esso collegati. Per saperne di più visiti hpo.jax.org.
- Versione dei dati 2026.10.21-777c9289.
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