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Egenskap
Increased calcium level in kidney
Klinisk navn: Nephrocalcinosis
Nephrocalcinosis is the deposition of calcium salts in renal parenchyma.
Sammendrag
- Også kalt
- Too much calcium deposited in kidneys
- Kroppssystem
- Abnormality of the genitourinary system
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Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/nephrocalcinosis.json"
page <- fromJSON(url)
page$trait$nameIncreased calcium level in kidneyHP:0000121
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Les genene knyttet til Increased calcium level in kidney, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test58 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.
- Inherited Parathyroid & Calcium-Sensing DisordersReads 6 of these genesCDC73GCM2CASRGNA11PTHGATA3About this report →
- Bartter DiseaseReads 4 of these genesKCNJ1SLC12A1BSNDCLCNKBAbout this report →
- Primary HyperoxaluriaReads 3 of these genesAGXTGRHPRHOGA1About this report →
- Dent Disease and Lowe SyndromeReads 2 of these genesCLCN5OCRLAbout this report →
Show 54 more reports
- Hypercalcemia InfantileReads 2 of these genesSLC34A1CYP24A1About this report →
- Thyroid CancerReads 7 of these genesCDC73GCM2MEN1CASRGNA11PTHAbout this report →
- Familial HypomagnesemiaReads 4 of these genesCLDN16CLDN19ATP1A1RRAGDAbout this report →
- Hereditary Arterial CalcificationReads 2 of these genesABCC6ENPP1About this report →
- Autoimmune Polyendocrine Syndrome Type 1 (APECED)Reads 1 of these genesAIREAbout this report →
- Familial Mediterranean FeverReads 1 of these genesMEFVAbout this report →
- HypophosphatasiaReads 1 of these genesALPLAbout this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- Renal Tubular AcidosisReads 2 of these genesATP6V0A4SLC4A1About this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 2 of these genesENPP1PHEXAbout this report →
- Malignant Endocrine NeoplasmReads 2 of these genesCDC73MEN1About this report →
- Pseudoxanthoma ElasticumReads 1 of these genesABCC6About this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesINSRAbout this report →
- Shwachman-Diamond SyndromeReads 1 of these genesSBDSAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 2 of these genesCDKN1CIGF2About this report →
- Severe Congenital NeutropeniaReads 2 of these genesCLPBSRP54About this report →
- Alport SyndromeReads 1 of these genesCOL4A3About this report →
- TyrosinemiaReads 1 of these genesFAHAbout this report →
- Congenital Diarrhoeas & EnteropathiesReads 2 of these genesMYO5BSTX3About this report →
- Glycogen Storage DiseaseReads 2 of these genesSLC2A2SLC37A4About this report →
- Cutis LaxaReads 2 of these genesATP6V1E1ELNAbout this report →
- Familial Atrial FibrillationReads 1 of these genesKCNQ1About this report →
- Familial Paget Disease of BoneReads 1 of these genesZNF687About this report →
- Fanconi Renotubular Syndrome and Renal GlucosuriaReads 1 of these genesHNF4AAbout this report →
- Short Qt SyndromeReads 1 of these genesKCNQ1About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Hereditary SpherocytosisReads 1 of these genesSLC4A1About this report →
- Rare Inherited Bone Marrow Failure SyndromesReads 1 of these genesDNAJC21About this report →
- Diabetes MellitusReads 2 of these genesSLC2A2HNF4AAbout this report →
- Hereditary Sideroblastic AnaemiasReads 1 of these genesTRNT1About this report →
- Purine & Pyrimidine Metabolism DisordersReads 1 of these genesHPRT1About this report →
- Red Blood Cell Membrane DisordersReads 1 of these genesSLC4A1About this report →
- Familial Intrahepatic CholestasisReads 1 of these genesMYO5BAbout this report →
- Long QT SyndromeReads 1 of these genesKCNQ1About this report →
- Congenital Disorders of GlycosylationReads 3 of these genesFUT8PIGTSLC37A4About this report →
- HyperinsulinismReads 1 of these genesINSRAbout this report →
- Epilepsy (Full Panel)Reads 4 of these genesSLC1A2ATP6V1B2STRADATBC1D24About this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesHNF4AAbout this report →
- Urea Cycle DisorderReads 1 of these genesSLC7A7About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesELNAbout this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 1 of these genesPEX3About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesHSD11B2About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesCDKN1CIGF2About this report →
- Amelogenesis ImperfectaReads 1 of these genesFAM20AAbout this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesATP1A1MPV17About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGTAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesSLC2A2About this report →
- Autoimmune DiseaseReads 1 of these genesAIREAbout this report →
- Primary Mitochondrial DiseaseReads 2 of these genesDNAJC30MPV17About this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Other Inborn Errors of ImmunityReads 2 of these genesNCF1SBDSAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPEX3About this report →
- Hearing Loss and DeafnessReads 1 of these genesTBC1D24About this report →
- Intellectual DisabilityReads 1 of these genesZFXAbout this report →
Les genene knyttet til Increased calcium level in kidney, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test97 gener knyttet til Increased calcium level in kidney
Endringer i disse genene forårsaker sjeldne tilstander der Increased calcium level in kidney forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| AGXTalanine--glyoxylate aminotransferase | Alltid | I 2 tilstander |
| AMMECR1AMMECR nuclear protein 1 | Alltid | I 1 tilstand |
| CLCN5Cl-/H+ antiporter 5 | Alltid | I 4 tilstander |
| CLDN16claudin 16 | Alltid | I 1 tilstand |
| CLDN19claudin 19 | Alltid | I 1 tilstand |
| PEX3peroxisomal biogenesis factor 3 | Alltid | I 1 tilstand |
| SLC34A1solute carrier family 34 member 1 | Alltid | I 1 tilstand |
| SPOUT1SPOUT domain containing methyltransferase 1 | Alltid | I 1 tilstand |
| TRA2Btransformer 2 beta homolog | Alltid | I 1 tilstand |
| ATP6V0A4ATPase H+ transporting V0 subunit a4 | Svært ofte (80–99 %) | I 1 tilstand |
| CDC73cell division cycle 73 | Svært ofte (80–99 %) | I 3 tilstander |
| CLPBClpB family mitochondrial disaggregase | Svært ofte (80–99 %) | I 1 tilstand |
| FAM20AFAM20A golgi associated secretory pathway pseudokinase | Svært ofte (80–99 %) | I 2 tilstander |
| GCM2GCM transcription factor 2 | Svært ofte (80–99 %) | I 1 tilstand |
| GRHPRglyoxylate and hydroxypyruvate reductase | Svært ofte (80–99 %) | I 2 tilstander |
| HOGA14-hydroxy-2-oxoglutarate aldolase 1 | Svært ofte (80–99 %) | I 1 tilstand |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Svært ofte (80–99 %) | I 1 tilstand |
| MEN1menin 1 | Svært ofte (80–99 %) | I 1 tilstand |
| SLC12A1solute carrier family 12 member 1 | Svært ofte (80–99 %) | I 1 tilstand |
| ABCC6ATP binding cassette subfamily C member 6 | Ofte (30–79 %) | I 3 tilstander |
| ATP1A1ATPase Na+/K+ transporting subunit alpha 1 | Ofte (30–79 %) | I 1 tilstand |
| ATP6V1E1ATPase H+ transporting V1 subunit E1 | Ofte (30–79 %) | I 1 tilstand |
| CASRcalcium sensing receptor | Ofte (30–79 %) | I 2 tilstander |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Ofte (30–79 %) | I 2 tilstander |
| FUT8fucosyltransferase 8 | Ofte (30–79 %) | I 1 tilstand |
| GEMIN4gem nuclear organelle associated protein 4 | Ofte (30–79 %) | I 1 tilstand |
| GNA11G protein subunit alpha 11 | Ofte (30–79 %) | I 1 tilstand |
| HPRT1hypoxanthine phosphoribosyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| HSD11B2hydroxysteroid 11-beta dehydrogenase 2 | Ofte (30–79 %) | I 1 tilstand |
| MYO5Bmyosin VB | Ofte (30–79 %) | I 1 tilstand |
| OXGR1oxoglutarate receptor 1 | Ofte (30–79 %) | I 1 tilstand |
| PHEXphosphate regulating endopeptidase X-linked | Ofte (30–79 %) | I 1 tilstand |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Ofte (30–79 %) | I 2 tilstander |
| PIK3C2Aphosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | Ofte (30–79 %) | I 1 tilstand |
| PTHparathyroid hormone | Ofte (30–79 %) | I 1 tilstand |
| ROR2ROR family WNT receptor 2 | Ofte (30–79 %) | I 1 tilstand |
| RRAGDRas related GTP binding D | Ofte (30–79 %) | I 2 tilstander |
| SLC1A2solute carrier family 1 member 2 | Ofte (30–79 %) | I 1 tilstand |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Ofte (30–79 %) | I 2 tilstander |
| SLC7A7solute carrier family 7 member 7 | Ofte (30–79 %) | I 1 tilstand |
Vis 57 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| STX3syntaxin 3 | Ofte (30–79 %) | I 1 tilstand |
| TRNT1tRNA nucleotidyl transferase 1 | Ofte (30–79 %) | I 1 tilstand |
| VPS33BVPS33B late endosome and lysosome associated | Ofte (30–79 %) | I 2 tilstander |
| AIREautoimmune regulator | Noen ganger (5–29 %) | I 1 tilstand |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Noen ganger (5–29 %) | I 1 tilstand |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Noen ganger (5–29 %) | I 1 tilstand |
| BSNDbarttin CLCNK type accessory subunit beta | Noen ganger (5–29 %) | I 1 tilstand |
| BTNL2butyrophilin like 2 | Noen ganger (5–29 %) | I 1 tilstand |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Noen ganger (5–29 %) | I 1 tilstand |
| CLCNKAchloride voltage-gated channel Ka | Noen ganger (5–29 %) | I 1 tilstand |
| CLCNKBchloride voltage-gated channel Kb | Noen ganger (5–29 %) | I 1 tilstand |
| CLIP2CAP-Gly domain containing linker protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Noen ganger (5–29 %) | I 1 tilstand |
| DYNC2I2dynein 2 intermediate chain 2 | Noen ganger (5–29 %) | I 1 tilstand |
| EIF4Heukaryotic translation initiation factor 4H | Noen ganger (5–29 %) | I 1 tilstand |
| ELNelastin | Noen ganger (5–29 %) | I 2 tilstander |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Noen ganger (5–29 %) | I 1 tilstand |
| GTF2Igeneral transcription factor IIi | Noen ganger (5–29 %) | I 1 tilstand |
| GTF2IRD1GTF2I repeat domain containing 1 | Noen ganger (5–29 %) | I 1 tilstand |
| GTF2IRD2GTF2I repeat domain containing 2 | Noen ganger (5–29 %) | I 1 tilstand |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Noen ganger (5–29 %) | I 1 tilstand |
| INSRinsulin receptor | Noen ganger (5–29 %) | I 2 tilstander |
| LIMK1LIM domain kinase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MEFVMEFV innate immunity regulator, pyrin | Noen ganger (5–29 %) | I 1 tilstand |
| METTL27methyltransferase like 27 | Noen ganger (5–29 %) | I 1 tilstand |
| MLXIPLMLX interacting protein like | Noen ganger (5–29 %) | I 1 tilstand |
| MPV17mitochondrial inner membrane protein MPV17 | Noen ganger (5–29 %) | I 1 tilstand |
| NCF1neutrophil cytosolic factor 1 | Noen ganger (5–29 %) | I 1 tilstand |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Noen ganger (5–29 %) | I 2 tilstander |
| PTH1Rparathyroid hormone 1 receptor | Noen ganger (5–29 %) | I 2 tilstander |
| RFC2replication factor C subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC2A2solute carrier family 2 member 2 | Noen ganger (5–29 %) | I 1 tilstand |
| SLC37A4solute carrier family 37 member 4 | Noen ganger (5–29 %) | I 1 tilstand |
| SRCAPSnf2 related CREBBP activator protein | Noen ganger (5–29 %) | I 2 tilstander |
| STRADASTE20 related adaptor alpha | Noen ganger (5–29 %) | I 2 tilstander |
| STX1Asyntaxin 1A | Noen ganger (5–29 %) | I 1 tilstand |
| TBC1D24TBC1 domain family member 24 | Noen ganger (5–29 %) | I 1 tilstand |
| TBL2transducin beta like 2 | Noen ganger (5–29 %) | I 1 tilstand |
| TMEM270transmembrane protein 270 | Noen ganger (5–29 %) | I 1 tilstand |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Noen ganger (5–29 %) | I 2 tilstander |
| VPS37DVPS37D subunit of ESCRT-I | Noen ganger (5–29 %) | I 1 tilstand |
| ZFXzinc finger protein X-linked | Noen ganger (5–29 %) | I 1 tilstand |
| ZNF687zinc finger protein 687 | Noen ganger (5–29 %) | I 1 tilstand |
| ALPLalkaline phosphatase, biomineralization associated | Ikke registrert | I 1 tilstand |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Ikke registrert | I 1 tilstand |
| COL4A3collagen type IV alpha 3 chain | Ikke registrert | I 1 tilstand |
| CYP24A1cytochrome P450 family 24 subfamily A member 1 | Ikke registrert | I 1 tilstand |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Ikke registrert | I 1 tilstand |
| FAHfumarylacetoacetate hydrolase | Ikke registrert | I 1 tilstand |
| GALNT3polypeptide N-acetylgalactosaminyltransferase 3 | Ikke registrert | I 1 tilstand |
| GATA3GATA binding protein 3 | Ikke registrert | I 1 tilstand |
| HNF4Ahepatocyte nuclear factor 4 alpha | Ikke registrert | I 1 tilstand |
| IGF2insulin like growth factor 2 | Ikke registrert | I 1 tilstand |
| KCNQ1potassium voltage-gated channel subfamily Q member 1 | Ikke registrert | I 1 tilstand |
| KCNQ1OT1KCNQ1 opposite strand/antisense transcript 1 | Ikke registrert | I 1 tilstand |
| SBDSSBDS ribosome maturation factor | Ikke registrert | I 1 tilstand |
| SRP54signal recognition particle 54 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
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Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.17-8666dff2.
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