Tunnus
Jaundice
Yellow pigmentation of the skin due to bilirubin, which in turn is the result of increased bilirubin concentration in the bloodstream.
Kokkuvõte
- Teised nimetused
- Yellow skin, Yellowing of the skin, Icterus
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Jaundice, and the rest of your genome, with one test.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test192 geeni on seotud tunnusega Jaundice
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Jaundice. 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 |
|---|---|---|
| ABCB11ATP binding cassette subfamily B member 11 | Alati | Esineb 3 haiguses |
| ABCB4ATP binding cassette subfamily B member 4 | Alati | Esineb 4 haiguses |
| ABCD3ATP binding cassette subfamily D member 3 | Alati | Esineb 1 haiguses |
| ALDOAaldolase, fructose-bisphosphate A | Alati | Esineb 1 haiguses |
| ATP11CATPase phospholipid transporting 11C (ATP11C blood group) | Alati | Esineb 1 haiguses |
| ATP8B1ATPase phospholipid transporting 8B1 | Alati | Esineb 4 haiguses |
| BAATbile acid-CoA:amino acid N-acyltransferase | Alati | Esineb 1 haiguses |
| CASKcalcium/calmodulin dependent serine protein kinase | Alati | Esineb 1 haiguses |
| CILK1ciliogenesis associated kinase 1 | Alati | Esineb 1 haiguses |
| CLDN1claudin 1 | Alati | Esineb 2 haiguses |
| COG7component of oligomeric golgi complex 7 | Alati | Esineb 2 haiguses |
| CYP7B1cytochrome P450 family 7 subfamily B member 1 | Alati | Esineb 2 haiguses |
| DCDC2doublecortin domain containing 2 | Alati | Esineb 1 haiguses |
| EPB42erythrocyte membrane protein band 4.2 | Alati | Esineb 2 haiguses |
| G6PDglucose-6-phosphate dehydrogenase | Alati | Esineb 1 haiguses |
| GALEUDP-galactose-4-epimerase | Alati | Esineb 1 haiguses |
| GALTgalactose-1-phosphate uridylyltransferase | Alati | Esineb 2 haiguses |
| HK1hexokinase 1 | Alati | Esineb 1 haiguses |
| IARS1isoleucyl-tRNA synthetase 1 | Alati | Esineb 1 haiguses |
| IFT56intraflagellar transport 56 | Alati | Esineb 1 haiguses |
| IL18BPinterleukin 18 binding protein | Alati | Esineb 1 haiguses |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Alati | Esineb 1 haiguses |
| KDM6Blysine demethylase 6B | Alati | Esineb 1 haiguses |
| KIF12kinesin family member 12 | Alati | Esineb 1 haiguses |
| KYNUkynureninase | Alati | Esineb 1 haiguses |
| LRRC7leucine rich repeat containing 7 | Alati | Esineb 1 haiguses |
| LSM7LSM7 homolog, U6 small nuclear RNA and mRNA degradation associated | Alati | Esineb 1 haiguses |
| LYNLYN proto-oncogene, Src family tyrosine kinase | Alati | Esineb 1 haiguses |
| MCCC1methylcrotonyl-CoA carboxylase subunit 1 | Alati | Esineb 1 haiguses |
| MED12mediator complex subunit 12 | Alati | Esineb 1 haiguses |
| PEX1peroxisomal biogenesis factor 1 | Alati | Esineb 2 haiguses |
| PEX14peroxisomal biogenesis factor 14 | Alati | Esineb 2 haiguses |
| PEX26peroxisomal biogenesis factor 26 | Alati | Esineb 2 haiguses |
| PKD2polycystin 2, transient receptor potential cation channel | Alati | Esineb 1 haiguses |
| PKLRpyruvate kinase L/R | Alati | Esineb 1 haiguses |
| POLG2DNA polymerase gamma 2, accessory subunit | Alati | Esineb 1 haiguses |
| PSKH1protein serine kinase H1 | Alati | Esineb 1 haiguses |
| PTCRApre T cell antigen receptor alpha | Alati | Esineb 1 haiguses |
| RNU6ATACRNA, U6atac small nuclear | Alati | Esineb 1 haiguses |
| SCO2synthesis of cytochrome C oxidase 2 | Alati | Esineb 1 haiguses |
Näita veel 152 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| SLC2A1solute carrier family 2 member 1 | Alati | Esineb 2 haiguses |
| SPTBspectrin beta, erythrocytic | Alati | Esineb 3 haiguses |
| TCP1t-complex 1 | Alati | Esineb 1 haiguses |
| TMEM63Btransmembrane protein 63B | Alati | Esineb 1 haiguses |
| TRMUtRNA mitochondrial 2-thiouridylase | Alati | Esineb 1 haiguses |
| UGT1A1UDP glucuronosyltransferase family 1 member A1 | Alati | Esineb 4 haiguses |
| UROSuroporphyrinogen III synthase | Alati | Esineb 1 haiguses |
| VPS33BVPS33B late endosome and lysosome associated | Alati | Esineb 2 haiguses |
| ABCC2ATP binding cassette subfamily C member 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ANK1ankyrin 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| ATP7BATPase copper transporting beta | Väga sageli (80–99%) | Esineb 2 haiguses |
| BRCA1BRCA1 DNA repair associated | Väga sageli (80–99%) | Esineb 2 haiguses |
| BRCA2BRCA2 DNA repair associated | Väga sageli (80–99%) | Esineb 2 haiguses |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Väga sageli (80–99%) | Esineb 2 haiguses |
| MYO5Bmyosin VB | Väga sageli (80–99%) | Esineb 1 haiguses |
| NKX2-5NK2 homeobox 5 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PAX8paired box 8 | Väga sageli (80–99%) | Esineb 2 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 |
| PEX16peroxisomal biogenesis factor 16 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PEX19peroxisomal biogenesis factor 19 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX2peroxisomal biogenesis factor 2 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PEX3peroxisomal biogenesis factor 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PEX5peroxisomal biogenesis factor 5 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PEX6peroxisomal biogenesis factor 6 | Väga sageli (80–99%) | Esineb 1 haiguses |
| PRF1perforin 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| PTPN3protein tyrosine phosphatase non-receptor type 3 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ROS1ROS proto-oncogene 1, receptor tyrosine kinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC25A13solute carrier family 25 member 13 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLC26A4solute carrier family 26 member 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SLCO1B1solute carrier organic anion transporter family member 1B1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SLCO1B3solute carrier organic anion transporter family member 1B3 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TSHRthyroid stimulating hormone receptor | Väga sageli (80–99%) | Esineb 1 haiguses |
| ADAMTS13ADAM metallopeptidase with thrombospondin type 1 motif 13 | Sageli (30–79%) | Esineb 1 haiguses |
| AKR1D1aldo-keto reductase family 1 member D1 | Sageli (30–79%) | Esineb 2 haiguses |
| ATP7AATPase copper transporting alpha | Sageli (30–79%) | Esineb 1 haiguses |
| CDKN2Acyclin dependent kinase inhibitor 2A | Sageli (30–79%) | Esineb 1 haiguses |
| DEF6DEF6 guanine nucleotide exchange factor | Sageli (30–79%) | Esineb 1 haiguses |
| FOCADfocadhesin | Sageli (30–79%) | Esineb 1 haiguses |
| GPIglucose-6-phosphate isomerase | Sageli (30–79%) | Esineb 2 haiguses |
| HBBhemoglobin subunit beta | Sageli (30–79%) | Esineb 5 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 |
| KRASKRas proto-oncogene, GTPase | 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 |
| MTR5-methyltetrahydrofolate-homocysteine methyltransferase | Sageli (30–79%) | Esineb 1 haiguses |
| NPC2NPC intracellular cholesterol transporter 2 | Sageli (30–79%) | Esineb 1 haiguses |
| NR1H4nuclear receptor subfamily 1 group H member 4 | Sageli (30–79%) | Esineb 2 haiguses |
| PALB2partner and localizer of BRCA2 | Sageli (30–79%) | Esineb 1 haiguses |
| PALLDpalladin, cytoskeletal associated protein | Sageli (30–79%) | Esineb 1 haiguses |
| PFKMphosphofructokinase, muscle | Sageli (30–79%) | Esineb 1 haiguses |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Sageli (30–79%) | Esineb 2 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 |
| RAB27ARAB27A, member RAS oncogene family | Sageli (30–79%) | Esineb 1 haiguses |
| RABL3RAB, member of RAS oncogene family like 3 | Sageli (30–79%) | Esineb 1 haiguses |
| RHAGRh associated glycoprotein | Sageli (30–79%) | Esineb 3 haiguses |
| SERPINA1serpin family A member 1 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Sageli (30–79%) | Esineb 3 haiguses |
| SMAD4SMAD family member 4 | Sageli (30–79%) | Esineb 1 haiguses |
| SPIBSpi-B transcription factor | Sageli (30–79%) | Esineb 1 haiguses |
| SPTA1spectrin alpha, erythrocytic 1 | Sageli (30–79%) | Esineb 2 haiguses |
| STX11syntaxin 11 | Sageli (30–79%) | Esineb 2 haiguses |
| TFAMtranscription factor A, mitochondrial | Sageli (30–79%) | Esineb 1 haiguses |
| TNFSF15TNF superfamily member 15 | Sageli (30–79%) | Esineb 1 haiguses |
| TNPO3transportin 3 | Sageli (30–79%) | Esineb 1 haiguses |
| TP53tumor protein p53 | Sageli (30–79%) | Esineb 1 haiguses |
| ZFYVE19zinc finger FYVE-type containing 19 | Sageli (30–79%) | Esineb 1 haiguses |
| ACADVLacyl-CoA dehydrogenase very long chain | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALDOBaldolase, fructose-bisphosphate B | Mõnikord (5–29%) | Esineb 2 haiguses |
| ALG6ALG6 alpha-1,3-glucosyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| CA5Acarbonic anhydrase 5A | Mõnikord (5–29%) | Esineb 1 haiguses |
| CALRcalreticulin | Mõnikord (5–29%) | Esineb 1 haiguses |
| CASRcalcium sensing receptor | Mõnikord (5–29%) | Esineb 1 haiguses |
| COX4I2cytochrome c oxidase subunit 4I2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CPA1carboxypeptidase A1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTRCchymotrypsin C | Mõnikord (5–29%) | Esineb 2 haiguses |
| DPAGT1dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DZIP1LDAZ interacting zinc finger protein 1 like | Mõnikord (5–29%) | Esineb 1 haiguses |
| EIF2AK3eukaryotic translation initiation factor 2 alpha kinase 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| EPB41erythrocyte membrane protein band 4.1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| F5coagulation factor V | Mõnikord (5–29%) | Esineb 1 haiguses |
| FCGR3BFc gamma receptor IIIb | Mõnikord (5–29%) | Esineb 1 haiguses |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| GCLCglutamate-cysteine ligase catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| GPR35G protein-coupled receptor 35 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GYPCglycophorin C (Gerbich blood group) | Mõnikord (5–29%) | Esineb 1 haiguses |
| HBG2hemoglobin subunit gamma 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Mõnikord (5–29%) | Esineb 1 haiguses |
| HNF1BHNF1 homeobox B | Mõnikord (5–29%) | Esineb 1 haiguses |
| HTRA2HtrA serine peptidase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| JAK2Janus kinase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LBRlamin B receptor | Mõnikord (5–29%) | Esineb 2 haiguses |
| LIPAlipase A, lysosomal acid type | Mõnikord (5–29%) | Esineb 1 haiguses |
| LRP5LDL receptor related protein 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LYSTlysosomal trafficking regulator | Mõnikord (5–29%) | Esineb 2 haiguses |
| MMACHCmetabolism of cobalamin associated C | Mõnikord (5–29%) | Esineb 1 haiguses |
| MST1macrophage stimulating 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Mõnikord (5–29%) | Esineb 1 haiguses |
| NEK8NIMA related kinase 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NPHP3nephrocystin 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| OPLAH5-oxoprolinase, ATP-hydrolysing | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRKCSHPRKCSH beta subunit of glucosidase II | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRSS1serine protease 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PRSS2serine protease 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| RHCERh blood group CcEe antigens | Mõnikord (5–29%) | Esineb 1 haiguses |
| RHDRh blood group D antigen | Mõnikord (5–29%) | Esineb 1 haiguses |
| SEC63SEC63 protein translocation regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| SEMA4Dsemaphorin 4D | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC30A10solute carrier family 30 member 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMPD1sphingomyelin phosphodiesterase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SP110SP110 nuclear body protein | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPINK1serine peptidase inhibitor Kazal type 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SPTBN1spectrin beta, non-erythrocytic 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| STXBP2syntaxin binding protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TCF4transcription factor 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRPV6transient receptor potential cation channel subfamily V member 6 | Mõnikord (5–29%) | Esineb 1 haiguses |
| UNC13Dunc-13 homolog D | Mõnikord (5–29%) | Esineb 1 haiguses |
| IL2RGinterleukin 2 receptor subunit gamma | Harva (1–4%) | Esineb 1 haiguses |
| ATP6AP2ATPase H+ transporting accessory protein 2 | Pole registreeritud | Esineb 1 haiguses |
| CDIN1CDAN1 interacting nuclease 1 | Pole registreeritud | Esineb 1 haiguses |
| CPOXcoproporphyrinogen oxidase | Pole registreeritud | Esineb 1 haiguses |
| DGUOKdeoxyguanosine kinase | Pole registreeritud | Esineb 1 haiguses |
| DHFRdihydrofolate reductase | Pole registreeritud | Esineb 1 haiguses |
| ETFAelectron transfer flavoprotein subunit alpha | Pole registreeritud | Esineb 1 haiguses |
| ETFBelectron transfer flavoprotein subunit beta | Pole registreeritud | Esineb 1 haiguses |
| ETFDHelectron transfer flavoprotein dehydrogenase | Pole registreeritud | Esineb 1 haiguses |
| GLRX5glutaredoxin 5 | Pole registreeritud | Esineb 1 haiguses |
| IER3IP1immediate early response 3 interacting protein 1 | Pole registreeritud | Esineb 1 haiguses |
| KCNN4potassium calcium-activated channel subfamily N member 4 | Pole registreeritud | Esineb 1 haiguses |
| KIF23kinesin family member 23 | Pole registreeritud | Esineb 1 haiguses |
| KRT18keratin 18 | Pole registreeritud | Esineb 1 haiguses |
| LPLlipoprotein lipase | Pole registreeritud | Esineb 1 haiguses |
| NBASNBAS subunit of NRZ tethering complex | Pole registreeritud | Esineb 1 haiguses |
| OCLNoccludin | Pole registreeritud | Esineb 1 haiguses |
| POU1F1POU class 1 homeobox 1 | Pole registreeritud | Esineb 1 haiguses |
| RINT1RAD50 interactor 1 | Pole registreeritud | Esineb 1 haiguses |
| SEC23BSEC23 homolog B, COPII component | Pole registreeritud | Esineb 1 haiguses |
| SKIC3SKI3 subunit of superkiller complex | Pole registreeritud | Esineb 1 haiguses |
| TBX19T-box transcription factor 19 | Pole registreeritud | Esineb 1 haiguses |
| TPI1triosephosphate isomerase 1 | Pole registreeritud | Esineb 1 haiguses |
| TULP3TUB like protein 3 | Pole registreeritud | Esineb 1 haiguses |
| USP53ubiquitin specific peptidase 53 | Pole registreeritud | Esineb 1 haiguses |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | 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