Tunnus
Liver failure
Kliiniline nimetus: Hepatic failure
Kokkuvõte
- Teised nimetused
- Hepatic insufficiency
- Kehasüsteem
- Abnormality of the digestive system
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Liver failure, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test141 geeni on seotud tunnusega Liver failure
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Liver failure. 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 |
|---|---|---|
| ABCD3ATP binding cassette subfamily D member 3 | Alati | Esineb 1 haiguses |
| APOA1apolipoprotein A1 | Alati | Esineb 1 haiguses |
| ATP7BATPase copper transporting beta | Alati | Esineb 1 haiguses |
| CYP7B1cytochrome P450 family 7 subfamily B member 1 | Alati | Esineb 2 haiguses |
| DCDC2doublecortin domain containing 2 | Alati | Esineb 1 haiguses |
| DGUOKdeoxyguanosine kinase | Alati | Esineb 1 haiguses |
| F8coagulation factor VIII | Alati | Esineb 1 haiguses |
| FAHfumarylacetoacetate hydrolase | Alati | Esineb 1 haiguses |
| FHfumarate hydratase | Alati | Esineb 1 haiguses |
| IL18BPinterleukin 18 binding protein | Alati | Esineb 1 haiguses |
| IL27RAinterleukin 27 receptor subunit alpha | Alati | Esineb 1 haiguses |
| LIPAlipase A, lysosomal acid type | Alati | Esineb 3 haiguses |
| MARS1methionyl-tRNA synthetase 1 | Alati | Esineb 1 haiguses |
| MRM2mitochondrial rRNA methyltransferase 2 | Alati | Esineb 1 haiguses |
| NR1H4nuclear receptor subfamily 1 group H member 4 | Alati | Esineb 1 haiguses |
| PCK1phosphoenolpyruvate carboxykinase 1 | Alati | Esineb 1 haiguses |
| PEX19peroxisomal biogenesis factor 19 | Alati | Esineb 2 haiguses |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Alati | Esineb 2 haiguses |
| POT1protection of telomeres 1 | Alati | Esineb 1 haiguses |
| PSKH1protein serine kinase H1 | Alati | Esineb 1 haiguses |
| RFC4replication factor C subunit 4 | Alati | Esineb 1 haiguses |
| TFAMtranscription factor A, mitochondrial | Alati | Esineb 1 haiguses |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Alati | Esineb 1 haiguses |
| CPT1Acarnitine palmitoyltransferase 1A | Väga sageli (80–99%) | Esineb 1 haiguses |
| OTCornithine transcarbamylase | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX1peroxisomal biogenesis factor 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX10peroxisomal biogenesis factor 10 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX11Bperoxisomal biogenesis factor 11 beta | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX12peroxisomal biogenesis factor 12 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX13peroxisomal biogenesis factor 13 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX14peroxisomal biogenesis factor 14 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX16peroxisomal biogenesis factor 16 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX2peroxisomal biogenesis factor 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX26peroxisomal biogenesis factor 26 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX3peroxisomal biogenesis factor 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX5peroxisomal biogenesis factor 5 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX6peroxisomal biogenesis factor 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SMPD1sphingomyelin phosphodiesterase 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ACTG2actin gamma 2, smooth muscle | Sageli (30–79%) | Esineb 1 haiguses |
| AKR1D1aldo-keto reductase family 1 member D1 | Sageli (30–79%) | Esineb 2 haiguses |
Näita veel 101 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| COX16cytochrome c oxidase assembly factor COX16 | Sageli (30–79%) | Esineb 1 haiguses |
| CPT2carnitine palmitoyltransferase 2 | Sageli (30–79%) | Esineb 2 haiguses |
| DEF6DEF6 guanine nucleotide exchange factor | Sageli (30–79%) | Esineb 1 haiguses |
| FOCADfocadhesin | Sageli (30–79%) | Esineb 1 haiguses |
| GALTgalactose-1-phosphate uridylyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| GFM1G elongation factor mitochondrial 1 | Sageli (30–79%) | Esineb 1 haiguses |
| H4C3H4 clustered histone 3 | Sageli (30–79%) | Esineb 1 haiguses |
| IL12Ainterleukin 12A | Sageli (30–79%) | Esineb 1 haiguses |
| IL12RB1interleukin 12 receptor subunit beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| IRF5interferon regulatory factor 5 | Sageli (30–79%) | Esineb 1 haiguses |
| MMEL1membrane metalloendopeptidase like 1 | Sageli (30–79%) | Esineb 1 haiguses |
| MPV17mitochondrial inner membrane protein MPV17 | Sageli (30–79%) | Esineb 1 haiguses |
| MRPS7mitochondrial ribosomal protein S7 | Sageli (30–79%) | Esineb 1 haiguses |
| POLGDNA polymerase gamma, catalytic subunit | Sageli (30–79%) | Esineb 1 haiguses |
| POU2AF1POU class 2 homeobox associating factor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| RBM10RNA binding motif protein 10 | Sageli (30–79%) | Esineb 1 haiguses |
| SC5Dsterol-C5-desaturase | Sageli (30–79%) | Esineb 1 haiguses |
| SERAC1serine active site containing 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC7A7solute carrier family 7 member 7 | Sageli (30–79%) | Esineb 1 haiguses |
| SPIBSpi-B transcription factor | Sageli (30–79%) | Esineb 1 haiguses |
| TJP2tight junction protein 2 | Sageli (30–79%) | Esineb 1 haiguses |
| TNFSF15TNF superfamily member 15 | Sageli (30–79%) | Esineb 1 haiguses |
| TNPO3transportin 3 | Sageli (30–79%) | Esineb 1 haiguses |
| VMA22vacuolar ATPase assembly factor VMA22 | Sageli (30–79%) | Esineb 1 haiguses |
| ACDACD shelterin complex subunit and telomerase recruitment factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| ACVRL1activin A receptor like type 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALMS1ALMS1 centrosome and basal body associated protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| ASLargininosuccinate lyase | Mõnikord (5–29%) | Esineb 1 haiguses |
| BAATbile acid-CoA:amino acid N-acyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| BTNL2butyrophilin like 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CILK1ciliogenesis associated kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CLDN1claudin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COG4component of oligomeric golgi complex 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTC1CST telomere replication complex component 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DKC1dyskerin pseudouridine synthase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DLDdihydrolipoamide dehydrogenase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ENGendoglin | Mõnikord (5–29%) | Esineb 1 haiguses |
| EPM2AEPM2A glucan phosphatase, laforin | Mõnikord (5–29%) | Esineb 2 haiguses |
| GDF2growth differentiation factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HLA-Bmajor histocompatibility complex, class I, B | Mõnikord (5–29%) | Esineb 1 haiguses |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| IARS1isoleucyl-tRNA synthetase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL21Rinterleukin 21 receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| JAG1jagged canonical Notch ligand 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MED12mediator complex subunit 12 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ATP6mitochondrially encoded ATP synthase membrane subunit 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ND2mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-ND3mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 3 | 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-TKmitochondrially encoded tRNA-Lys (AAA/G) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Mõnikord (5–29%) | Esineb 1 haiguses |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Mõnikord (5–29%) | Esineb 1 haiguses |
| NHLRC1NHL repeat containing E3 ubiquitin protein ligase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NHP2NHP2 ribonucleoprotein | Mõnikord (5–29%) | Esineb 1 haiguses |
| NOP10NOP10 ribonucleoprotein | Mõnikord (5–29%) | Esineb 1 haiguses |
| NPM1nucleophosmin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PARNpoly(A)-specific ribonuclease | Mõnikord (5–29%) | Esineb 1 haiguses |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RTEL1regulator of telomere elongation helicase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SH2D1ASH2 domain containing 1A | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC25A20solute carrier family 25 member 20 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC2A2solute carrier family 2 member 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMAD4SMAD family member 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TERCtelomerase RNA component | Mõnikord (5–29%) | Esineb 1 haiguses |
| TERTtelomerase reverse transcriptase | Mõnikord (5–29%) | Esineb 1 haiguses |
| TINF2TERF1 interacting nuclear factor 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TYMSthymidylate synthetase | Mõnikord (5–29%) | Esineb 1 haiguses |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| WRAP53WD repeat containing antisense to TP53 | Mõnikord (5–29%) | Esineb 1 haiguses |
| XIAPX-linked inhibitor of apoptosis | Mõnikord (5–29%) | Esineb 2 haiguses |
| ASAH1N-acylsphingosine amidohydrolase 1 | Harva (1–4%) | Esineb 1 haiguses |
| ATRXATRX chromatin remodeler | Harva (1–4%) | Esineb 1 haiguses |
| F13A1coagulation factor XIII A chain | Harva (1–4%) | Esineb 1 haiguses |
| F13Bcoagulation factor XIII B chain | Harva (1–4%) | Esineb 1 haiguses |
| GBA1glucosylceramidase beta 1 | Harva (1–4%) | Esineb 2 haiguses |
| MAP2K1mitogen-activated protein kinase kinase 1 | Harva (1–4%) | Esineb 1 haiguses |
| NRASNRAS proto-oncogene, GTPase | Harva (1–4%) | Esineb 1 haiguses |
| RYR1ryanodine receptor 1 | Harva (1–4%) | Esineb 1 haiguses |
| SCARB2scavenger receptor class B member 2 | Harva (1–4%) | Esineb 1 haiguses |
| SLC25A15solute carrier family 25 member 15 | Harva (1–4%) | Esineb 1 haiguses |
| ACAD9acyl-CoA dehydrogenase family member 9 | Pole registreeritud | Esineb 1 haiguses |
| AMACRalpha-methylacyl-CoA racemase | Pole registreeritud | Esineb 1 haiguses |
| APTXaprataxin | Pole registreeritud | Esineb 1 haiguses |
| COQ2coenzyme Q2, polyprenyltransferase | Pole registreeritud | Esineb 1 haiguses |
| FECHferrochelatase | Pole registreeritud | Esineb 1 haiguses |
| GBE11,4-alpha-glucan branching enzyme 1 | Pole registreeritud | Esineb 1 haiguses |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Pole registreeritud | Esineb 1 haiguses |
| IFT122intraflagellar transport 122 | Pole registreeritud | Esineb 1 haiguses |
| IFT172intraflagellar transport 172 | Pole registreeritud | Esineb 1 haiguses |
| MPImannose phosphate isomerase | Pole registreeritud | Esineb 1 haiguses |
| NDUFS4NADH:ubiquinone oxidoreductase subunit S4 | Pole registreeritud | Esineb 1 haiguses |
| OSTM1osteoclastogenesis associated transmembrane protein 1 | Pole registreeritud | Esineb 1 haiguses |
| PCK2phosphoenolpyruvate carboxykinase 2, mitochondrial | Pole registreeritud | Esineb 1 haiguses |
| SCYL1SCY1 like pseudokinase 1 | Pole registreeritud | Esineb 1 haiguses |
| SKIC3SKI3 subunit of superkiller complex | 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