Tunnus
Kidney damage
Kliiniline nimetus: Nephropathy
A nonspecific term referring to disease or damage of the kidneys.
Kokkuvõte
- Teised nimetused
- Kidney disease
- Kehasüsteem
- Abnormality of the genitourinary system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Kidney damage, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test103 geeni on seotud tunnusega Kidney damage
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Kidney damage. 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 |
|---|---|---|
| IFT140intraflagellar transport 140 | Alati | Esineb 2 haiguses |
| INPP5Einositol polyphosphate-5-phosphatase E | Alati | Esineb 2 haiguses |
| JKAMPJNK1/MAPK8 associated membrane protein | Alati | Esineb 1 haiguses |
| PSKH1protein serine kinase H1 | Alati | Esineb 1 haiguses |
| SEC61A1SEC61 translocon subunit alpha 1 | Alati | Esineb 1 haiguses |
| SLC5A2solute carrier family 5 member 2 | Alati | Esineb 1 haiguses |
| CC2D2Acoiled-coil and C2 domain containing 2A | Väga sageli (80–99%) | Esineb 2 haiguses |
| CEP290centrosomal protein 290 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CLDN19claudin 19 | Väga sageli (80–99%) | Esineb 1 haiguses |
| FAM20AFAM20A golgi associated secretory pathway pseudokinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| GON7GON7 subunit of KEOPS complex | Väga sageli (80–99%) | Esineb 1 haiguses |
| LAGE3L antigen family member 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NPHP1nephrocystin 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NUP107nucleoporin 107 | Väga sageli (80–99%) | Esineb 1 haiguses |
| NUP133nucleoporin 133 | Väga sageli (80–99%) | Esineb 1 haiguses |
| OSGEPO-sialoglycoprotein endopeptidase | Väga sageli (80–99%) | Esineb 1 haiguses |
| RPGRIP1LRPGRIP1 like | Väga sageli (80–99%) | Esineb 2 haiguses |
| SAA1serum amyloid A1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TMEM138transmembrane protein 138 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TMEM216transmembrane protein 216 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TMEM231transmembrane protein 231 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TMEM237transmembrane protein 237 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TP53RKTP53 regulating kinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| TPRKBTP53RK binding protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| TTRtransthyretin | Väga sageli (80–99%) | Esineb 1 haiguses |
| WDR4WDR4 tRNA N7-guanosine methyltransferase non-catalytic subunit | Väga sageli (80–99%) | Esineb 1 haiguses |
| WDR73WD repeat domain 73 | Väga sageli (80–99%) | Esineb 1 haiguses |
| WT1WT1 transcription factor | Väga sageli (80–99%) | Esineb 3 haiguses |
| YRDCyrdC N6-threonylcarbamoyltransferase domain containing | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZNF423zinc finger protein 423 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CCND1cyclin D1 | Sageli (30–79%) | Esineb 1 haiguses |
| CISD2CDGSH iron sulfur domain 2 | Sageli (30–79%) | Esineb 1 haiguses |
| COL4A5collagen type IV alpha 5 chain | Sageli (30–79%) | Esineb 1 haiguses |
| COL4A6collagen type IV alpha 6 chain | Sageli (30–79%) | Esineb 1 haiguses |
| GLAgalactosidase alpha | Sageli (30–79%) | Esineb 1 haiguses |
| HPRT1hypoxanthine phosphoribosyltransferase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MAFBMAF bZIP transcription factor B | Sageli (30–79%) | Esineb 1 haiguses |
| MYH9myosin heavy chain 9 | Sageli (30–79%) | Esineb 1 haiguses |
| NLRP3NLR family pyrin domain containing 3 | Sageli (30–79%) | Esineb 1 haiguses |
Näita veel 63 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| PRODHproline dehydrogenase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SCNN1Asodium channel epithelial 1 subunit alpha | Sageli (30–79%) | Esineb 1 haiguses |
| SCNN1Bsodium channel epithelial 1 subunit beta | Sageli (30–79%) | Esineb 1 haiguses |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Sageli (30–79%) | Esineb 1 haiguses |
| TMEM67transmembrane protein 67 | Sageli (30–79%) | Esineb 1 haiguses |
| TREX1three prime repair exonuclease 1 | Sageli (30–79%) | Esineb 1 haiguses |
| WFS1wolframin ER transmembrane glycoprotein | Sageli (30–79%) | Esineb 1 haiguses |
| ABCC8ATP binding cassette subfamily C member 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ADA2adenosine deaminase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| APPL1adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CELcarboxyl ester lipase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CEP120centrosomal protein 120 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CPOXcoproporphyrinogen oxidase | Mõnikord (5–29%) | Esineb 1 haiguses |
| DYNC2H1dynein cytoplasmic 2 heavy chain 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DYNC2I1dynein 2 intermediate chain 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DYNC2I2dynein 2 intermediate chain 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FOXI1forkhead box I1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GCKglucokinase | Mõnikord (5–29%) | Esineb 1 haiguses |
| HIC1HIC ZBTB transcriptional repressor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNF1AHNF1 homeobox A | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNF4Ahepatocyte nuclear factor 4 alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| IFT172intraflagellar transport 172 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IFT80intraflagellar transport 80 | Mõnikord (5–29%) | Esineb 1 haiguses |
| INSinsulin | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNJ10potassium inwardly rectifying channel subfamily J member 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KCNJ11potassium inwardly rectifying channel subfamily J member 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KIAA0753KIAA0753 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KLF11KLF transcription factor 11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MEFVMEFV innate immunity regulator, pyrin | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ND4mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Mõnikord (5–29%) | Esineb 1 haiguses |
| NEUROD1neuronal differentiation 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NOD2nucleotide binding oligomerization domain containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PAFAH1B1platelet activating factor acetylhydrolase 1b regulatory subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PAX4paired box 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PDX1pancreatic and duodenal homeobox 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC26A4solute carrier family 26 member 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC2A2solute carrier family 2 member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TTC21Btetratricopeptide repeat domain 21B | Mõnikord (5–29%) | Esineb 1 haiguses |
| WASWASP actin nucleation promoting factor | Mõnikord (5–29%) | Esineb 2 haiguses |
| WDR19WD repeat domain 19 | Mõnikord (5–29%) | Esineb 1 haiguses |
| YWHAEtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon | Mõnikord (5–29%) | Esineb 1 haiguses |
| FGAfibrinogen alpha chain | Pole registreeritud | Esineb 1 haiguses |
| MMACHCmetabolism of cobalamin associated C | Pole registreeritud | Esineb 1 haiguses |
| PAX6paired box 6 | Pole registreeritud | Esineb 1 haiguses |
| PRDX1peroxiredoxin 1 | Pole registreeritud | Esineb 1 haiguses |
| SCARB2scavenger receptor class B member 2 | Pole registreeritud | Esineb 1 haiguses |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Pole registreeritud | Esineb 1 haiguses |
| VPS33BVPS33B late endosome and lysosome associated | 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.
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