Tunnus
Corneal opacity
A reduction of corneal clarity.
Kokkuvõte
- Teised nimetused
- Corneal clouding, Corneal opacities, Reduction of corneal clarity, Scarring or clouding of the cornea of the eye
- Kehasüsteem
- Abnormality of the eye
VõrdlusgenoomGRCh38hg38
Geeni- ja variandilehtede positsioonid järgivad seda valikut selles brauseris.
Read the genes linked to Corneal opacity, and the rest of your genome, with one test.
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Telli oma Genome Test166 geeni on seotud tunnusega Corneal opacity
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Corneal opacity. 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 |
|---|---|---|
| ALDH18A1aldehyde dehydrogenase 18 family member A1 | Alati | Esineb 2 haiguses |
| ARSBarylsulfatase B | Alati | Esineb 1 haiguses |
| B3GALT6beta-1,3-galactosyltransferase 6 | Alati | Esineb 1 haiguses |
| BUD13BUD13 spliceosome associated protein | Alati | Esineb 1 haiguses |
| CHUKcomponent of inhibitor of nuclear factor kappa B kinase complex | Alati | Esineb 1 haiguses |
| FKRPfukutin related protein | Alati | Esineb 3 haiguses |
| FKTNfukutin | Alati | Esineb 2 haiguses |
| HYAL2hyaluronidase 2 | Alati | Esineb 1 haiguses |
| IDUAalpha-L-iduronidase | Alati | Esineb 6 haiguses |
| KERAkeratocan | Alati | Esineb 1 haiguses |
| LARGE1LARGE xylosyl- and glucuronyltransferase 1 | Alati | Esineb 2 haiguses |
| NDPnorrin cystine knot growth factor NDP | Alati | Esineb 3 haiguses |
| NGLY1N-glycanase 1 | Alati | Esineb 1 haiguses |
| PLCB3phospholipase C beta 3 | Alati | Esineb 1 haiguses |
| POMT1protein O-mannosyltransferase 1 | Alati | Esineb 2 haiguses |
| POMT2protein O-mannosyltransferase 2 | Alati | Esineb 2 haiguses |
| PXDNperoxidasin | Alati | Esineb 1 haiguses |
| RBM8ARNA binding motif protein 8A | Alati | Esineb 1 haiguses |
| TGFBItransforming growth factor beta induced | Alati | Esineb 2 haiguses |
| AGBL1AGBL carboxypeptidase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ATOH7atonal bHLH transcription factor 7 | Väga sageli (80–99%) | Esineb 2 haiguses |
| B3GLCTbeta 3-glucosyltransferase | Väga sageli (80–99%) | Esineb 1 haiguses |
| BMP4bone morphogenetic protein 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| BUB1BUB1 mitotic checkpoint serine/threonine kinase | Väga sageli (80–99%) | Esineb 1 haiguses |
| BUB1BBUB1 mitotic checkpoint serine/threonine kinase B | Väga sageli (80–99%) | Esineb 1 haiguses |
| BUB3BUB3 mitotic checkpoint protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| CEP57centrosomal protein 57 | Väga sageli (80–99%) | Esineb 1 haiguses |
| COL11A1collagen type XI alpha 1 chain | Väga sageli (80–99%) | Esineb 1 haiguses |
| COL8A2collagen type VIII alpha 2 chain | Väga sageli (80–99%) | Esineb 3 haiguses |
| COX7Bcytochrome c oxidase subunit 7B | Väga sageli (80–99%) | Esineb 1 haiguses |
| CTSAcathepsin A | Väga sageli (80–99%) | Esineb 1 haiguses |
| FOXE3forkhead box E3 | Väga sageli (80–99%) | Esineb 2 haiguses |
| FZD4frizzled class receptor 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GLAgalactosidase alpha | Väga sageli (80–99%) | Esineb 1 haiguses |
| GUSBglucuronidase beta | Väga sageli (80–99%) | Esineb 2 haiguses |
| HCCSholocytochrome c synthase | Väga sageli (80–99%) | Esineb 1 haiguses |
| LCATlecithin-cholesterol acyltransferase | Väga sageli (80–99%) | Esineb 1 haiguses |
| MAB21L1mab-21 like 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| MCOLN1mucolipin TRP cation channel 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Väga sageli (80–99%) | Esineb 1 haiguses |
Näita veel 126 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| NEU1neuraminidase 1 | Väga sageli (80–99%) | Esineb 3 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 |
| PEX19peroxisomal biogenesis factor 19 | 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 |
| SLC4A11solute carrier family 4 member 11 | Väga sageli (80–99%) | Esineb 3 haiguses |
| TATtyrosine aminotransferase | Väga sageli (80–99%) | Esineb 1 haiguses |
| TCF4transcription factor 4 | Väga sageli (80–99%) | Esineb 2 haiguses |
| TRIP13thyroid hormone receptor interactor 13 | Väga sageli (80–99%) | Esineb 1 haiguses |
| ZEB1zinc finger E-box binding homeobox 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| B3GALNT2beta-1,3-N-acetylgalactosaminyltransferase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| B4GAT1beta-1,4-glucuronyltransferase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| COL4A1collagen type IV alpha 1 chain | Sageli (30–79%) | Esineb 2 haiguses |
| CRPPACDP-L-ribitol pyrophosphorylase A | Sageli (30–79%) | Esineb 1 haiguses |
| CYP1B1cytochrome P450 family 1 subfamily B member 1 | Sageli (30–79%) | Esineb 2 haiguses |
| DAG1dystroglycan 1 | Sageli (30–79%) | Esineb 1 haiguses |
| DNA2DNA replication helicase/nuclease 2 | Sageli (30–79%) | Esineb 1 haiguses |
| FGFR1fibroblast growth factor receptor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| FOXC1forkhead box C1 | Sageli (30–79%) | Esineb 1 haiguses |
| FUCA1alpha-L-fucosidase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GBA1glucosylceramidase beta 1 | Sageli (30–79%) | Esineb 2 haiguses |
| GLB1galactosidase beta 1 | Sageli (30–79%) | Esineb 1 haiguses |
| GON4Lgon-4 like | Sageli (30–79%) | Esineb 1 haiguses |
| IKBKGinhibitor of nuclear factor kappa B kinase regulatory subunit gamma | Sageli (30–79%) | Esineb 1 haiguses |
| KRASKRas proto-oncogene, GTPase | Sageli (30–79%) | Esineb 2 haiguses |
| LRP5LDL receptor related protein 5 | Sageli (30–79%) | Esineb 1 haiguses |
| LTBP2latent transforming growth factor beta binding protein 2 | Sageli (30–79%) | Esineb 2 haiguses |
| MAFBMAF bZIP transcription factor B | Sageli (30–79%) | Esineb 1 haiguses |
| MMP2matrix metallopeptidase 2 | Sageli (30–79%) | Esineb 1 haiguses |
| MYOCmyocilin | Sageli (30–79%) | Esineb 1 haiguses |
| NEUROG1neurogenin 1 | Sageli (30–79%) | Esineb 1 haiguses |
| PAX6paired box 6 | Sageli (30–79%) | Esineb 2 haiguses |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Sageli (30–79%) | Esineb 1 haiguses |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Sageli (30–79%) | Esineb 1 haiguses |
| PLXND1plexin D1 | Sageli (30–79%) | Esineb 1 haiguses |
| POLR3ARNA polymerase III subunit A | Sageli (30–79%) | Esineb 1 haiguses |
| POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Sageli (30–79%) | Esineb 1 haiguses |
| POMGNT2protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) | Sageli (30–79%) | Esineb 1 haiguses |
| POMKprotein O-mannose kinase | Sageli (30–79%) | Esineb 1 haiguses |
| REV3LREV3 like, DNA directed polymerase zeta catalytic subunit | Sageli (30–79%) | Esineb 1 haiguses |
| RIPK4receptor interacting serine/threonine kinase 4 | Sageli (30–79%) | Esineb 1 haiguses |
| RXYLT1ribitol xylosyltransferase 1 | Sageli (30–79%) | Esineb 1 haiguses |
| ST14ST14 transmembrane serine protease matriptase | Sageli (30–79%) | Esineb 1 haiguses |
| STSsteroid sulfatase | Sageli (30–79%) | Esineb 1 haiguses |
| SUMF1sulfatase modifying factor 1 | Sageli (30–79%) | Esineb 2 haiguses |
| TEKTEK receptor tyrosine kinase | Sageli (30–79%) | Esineb 1 haiguses |
| TRIM44TRIM family member 44 | Sageli (30–79%) | Esineb 1 haiguses |
| TWIST2twist family bHLH transcription factor 2 | Sageli (30–79%) | Esineb 1 haiguses |
| ABCA1ATP binding cassette subfamily A member 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ASAH1N-acylsphingosine amidohydrolase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATAD3AATPase family AAA domain containing 3A | Mõnikord (5–29%) | Esineb 2 haiguses |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Mõnikord (5–29%) | Esineb 1 haiguses |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Mõnikord (5–29%) | Esineb 1 haiguses |
| CLIP2CAP-Gly domain containing linker protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COLEC10collectin subfamily member 10 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRYAAcrystallin alpha A | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRYBA4crystallin beta A4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRYBB1crystallin beta B1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRYBB2crystallin beta B2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRYGCcrystallin gamma C | Mõnikord (5–29%) | Esineb 1 haiguses |
| CRYGDcrystallin gamma D | Mõnikord (5–29%) | Esineb 1 haiguses |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Mõnikord (5–29%) | Esineb 1 haiguses |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Mõnikord (5–29%) | Esineb 1 haiguses |
| EIF4Heukaryotic translation initiation factor 4H | Mõnikord (5–29%) | Esineb 1 haiguses |
| ELNelastin | Mõnikord (5–29%) | Esineb 2 haiguses |
| ELP1elongator acetyltransferase complex subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FBLN5fibulin 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FERMT1FERM domain containing kindlin 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Mõnikord (5–29%) | Esineb 1 haiguses |
| GJA1gap junction protein alpha 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GJA8gap junction protein alpha 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GJB3gap junction protein beta 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GJB4gap junction protein beta 4 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| GTF2Igeneral transcription factor IIi | Mõnikord (5–29%) | Esineb 1 haiguses |
| GTF2IRD1GTF2I repeat domain containing 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GTF2IRD2GTF2I repeat domain containing 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HRASHRas proto-oncogene, GTPase | Mõnikord (5–29%) | Esineb 1 haiguses |
| KDSR3-ketodihydrosphingosine reductase | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRT14keratin 14 | Mõnikord (5–29%) | Esineb 1 haiguses |
| KRT5keratin 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LIMK1LIM domain kinase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| LMNAlamin A/C | Mõnikord (5–29%) | Esineb 1 haiguses |
| MAFMAF bZIP transcription factor | Mõnikord (5–29%) | Esineb 2 haiguses |
| MAN2B1mannosidase alpha class 2B member 1 | Mõnikord (5–29%) | Esineb 2 haiguses |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| METTL27methyltransferase like 27 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NCF1neutrophil cytosolic factor 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| NRASNRAS proto-oncogene, GTPase | Mõnikord (5–29%) | Esineb 1 haiguses |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Mõnikord (5–29%) | Esineb 1 haiguses |
| OTUD5OTU deubiquitinase 5 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PCYT1Aphosphate cytidylyltransferase 1A, choline | Mõnikord (5–29%) | Esineb 2 haiguses |
| PDGFRBplatelet derived growth factor receptor beta | Mõnikord (5–29%) | Esineb 1 haiguses |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PORCNporcupine O-acyltransferase | Mõnikord (5–29%) | Esineb 1 haiguses |
| PPP1R13Lprotein phosphatase 1 regulatory subunit 13 like | Mõnikord (5–29%) | Esineb 1 haiguses |
| RFC2replication factor C subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| STX1Asyntaxin 1A | Mõnikord (5–29%) | Esineb 1 haiguses |
| TBCEtubulin folding cofactor E | Mõnikord (5–29%) | Esineb 1 haiguses |
| TBCKTBC1 domain containing kinase | Mõnikord (5–29%) | Esineb 2 haiguses |
| TBL2transducin beta like 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TMEM270transmembrane protein 270 | Mõnikord (5–29%) | Esineb 1 haiguses |
| TRPV3transient receptor potential cation channel subfamily V member 3 | Mõnikord (5–29%) | Esineb 1 haiguses |
| VPS37DVPS37D subunit of ESCRT-I | Mõnikord (5–29%) | Esineb 1 haiguses |
| YAP1Yes1 associated transcriptional regulator | Mõnikord (5–29%) | Esineb 1 haiguses |
| ZMPSTE24zinc metallopeptidase STE24 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Harva (1–4%) | Esineb 1 haiguses |
| GRHL2grainyhead like transcription factor 2 | Harva (1–4%) | Esineb 1 haiguses |
| MT-CYBmitochondrially encoded cytochrome b | Harva (1–4%) | Esineb 1 haiguses |
| OVOL2ovo like zinc finger 2 | Harva (1–4%) | Esineb 2 haiguses |
| VSX1visual system homeobox 1 | Harva (1–4%) | Esineb 1 haiguses |
| DYMdymeclin | Pole registreeritud | Esineb 1 haiguses |
| FLNBfilamin B | Pole registreeritud | Esineb 1 haiguses |
| FRAS1Fraser extracellular matrix complex subunit 1 | Pole registreeritud | Esineb 1 haiguses |
| KIF11kinesin family member 11 | 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