Tunnus
Low blood potassium levels
Kliiniline nimetus: Hypokalemia
The concentration of potassium(1+) in the blood circulation is below the lower limit of normal.
Kokkuvõte
- Teised nimetused
- 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
- Kehasüsteem
- Laboratory abnormality
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Low blood potassium levels, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test62 geeni on seotud tunnusega Low blood potassium levels
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Low blood potassium levels. 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 |
|---|---|---|
| ATP1A1ATPase Na+/K+ transporting subunit alpha 1 | Alati | Esineb 1 haiguses |
| BSNDbarttin CLCNK type accessory subunit beta | Alati | Esineb 2 haiguses |
| CACNA1Dcalcium voltage-gated channel subunit alpha1 D | Alati | Esineb 2 haiguses |
| CACNA1Scalcium voltage-gated channel subunit alpha1 S | Alati | Esineb 2 haiguses |
| CLCN2chloride voltage-gated channel 2 | Alati | Esineb 2 haiguses |
| CLCNKBchloride voltage-gated channel Kb | Alati | Esineb 4 haiguses |
| CTNScystinosin, lysosomal cystine transporter | Alati | Esineb 3 haiguses |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Alati | Esineb 1 haiguses |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Alati | Esineb 2 haiguses |
| KCNJ18potassium inwardly rectifying channel subfamily J member 18 | Alati | Esineb 1 haiguses |
| NHEJ1non-homologous end joining factor 1 | Alati | Esineb 1 haiguses |
| PKD2polycystin 2, transient receptor potential cation channel | Alati | Esineb 1 haiguses |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Alati | Esineb 3 haiguses |
| SCNN1Asodium channel epithelial 1 subunit alpha | Alati | Esineb 2 haiguses |
| SCNN1Bsodium channel epithelial 1 subunit beta | Alati | Esineb 2 haiguses |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Alati | Esineb 2 haiguses |
| SERPINA6serpin family A member 6 | Alati | Esineb 1 haiguses |
| SLC12A1solute carrier family 12 member 1 | Alati | Esineb 1 haiguses |
| SLC26A3solute carrier family 26 member 3 | Alati | Esineb 1 haiguses |
| SLC4A4solute carrier family 4 member 4 | Alati | Esineb 1 haiguses |
| ATP6V0A4ATPase H+ transporting V0 subunit a4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ATP6V1B1ATPase H+ transporting V1 subunit B1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CLCNKAchloride voltage-gated channel Ka | Väga sageli (80–99%) | Esineb 2 haiguses |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Väga sageli (80–99%) | Esineb 3 haiguses |
| HSD11B2hydroxysteroid 11-beta dehydrogenase 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SLC12A3solute carrier family 12 member 3 | Väga sageli (80–99%) | Esineb 2 haiguses |
| CDKN2Acyclin dependent kinase inhibitor 2A | Sageli (30–79%) | Esineb 1 haiguses |
| CTNNB1catenin beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DEF6DEF6 guanine nucleotide exchange factor | Sageli (30–79%) | Esineb 1 haiguses |
| EHHADHenoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase | Sageli (30–79%) | Esineb 1 haiguses |
| FXYD2FXYD domain containing ion transport regulator 2 | Sageli (30–79%) | Esineb 1 haiguses |
| GATMglycine amidinotransferase | Sageli (30–79%) | Esineb 1 haiguses |
| GEMIN4gem nuclear organelle associated protein 4 | Sageli (30–79%) | Esineb 1 haiguses |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Sageli (30–79%) | Esineb 1 haiguses |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| NUP214nucleoporin 214 | Sageli (30–79%) | Esineb 1 haiguses |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Sageli (30–79%) | Esineb 1 haiguses |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 22 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| RRAGDRas related GTP binding D | Sageli (30–79%) | Esineb 1 haiguses |
| SLC34A1solute carrier family 34 member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| TERTtelomerase reverse transcriptase | Sageli (30–79%) | Esineb 1 haiguses |
| TP53tumor protein p53 | Sageli (30–79%) | Esineb 1 haiguses |
| ZNRF3zinc and ring finger 3 | Sageli (30–79%) | Esineb 1 haiguses |
| ASLargininosuccinate lyase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CASRcalcium sensing receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| CDH23cadherin related 23 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| H6PDhexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| HSD11B1hydroxysteroid 11-beta dehydrogenase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| INSRinsulin receptor | Mõnikord (5–29%) | Esineb 2 haiguses |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Mõnikord (5–29%) | Esineb 2 haiguses |
| UNC45Aunc-45 myosin chaperone A | Mõnikord (5–29%) | Esineb 1 haiguses |
| AIPAHR interacting HSP90 co-chaperone | Pole registreeritud | Esineb 1 haiguses |
| BMPR1Abone morphogenetic protein receptor type 1A | Pole registreeritud | Esineb 1 haiguses |
| CLDN10claudin 10 | Pole registreeritud | Esineb 1 haiguses |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Pole registreeritud | Esineb 1 haiguses |
| MAGED2MAGE family member D2 | Pole registreeritud | Esineb 1 haiguses |
| SLC2A2solute carrier family 2 member 2 | Pole registreeritud | Esineb 1 haiguses |
| SMAD4SMAD family member 4 | Pole registreeritud | Esineb 1 haiguses |
| USP8ubiquitin specific peptidase 8 | 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