Cecha
Astigmatism
A type of refraction error associated with abnormal curvatures on the anterior and/or posterior surface of the cornea.
Podsumowanie
- Znana także jako
- Abnormal curving of the cornea or lens of the eye
- Układ organizmu
- Abnormality of the eye
Genom referencyjnyGRCh38hg38
Pozycje na stronach genów i wariantów zależą od tego wyboru, w tej przeglądarce.
Read the genes linked to Astigmatism, and the rest of your genome, with one test.
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Zamawiam Genome Test221 genów powiązanych z Astigmatism
Zmiany w tych genach powodują rzadkie choroby, w których występuje Astigmatism. Większość osób z tą cechą nie ma żadnej z tych chorób, a gen z tej listy nic nie mówi o czyimkolwiek własnym genomie.
| Gen | Jak często występuje | Choroby |
|---|---|---|
| AHDC1AT-hook DNA binding motif containing 1 | Zawsze | W 1 chorobie |
| ARHGEF2Rho/Rac guanine nucleotide exchange factor 2 | Zawsze | W 1 chorobie |
| ARL6ARF like GTPase 6 | Zawsze | W 2 chorobach |
| BBS1Bardet-Biedl syndrome 1 | Zawsze | W 2 chorobach |
| CACNA1Fcalcium voltage-gated channel subunit alpha1 F | Zawsze | W 3 chorobach |
| CCDC28Bcoiled-coil domain containing 28B | Zawsze | W 1 chorobie |
| CLDN11claudin 11 | Zawsze | W 1 chorobie |
| COL9A1collagen type IX alpha 1 chain | Zawsze | W 1 chorobie |
| COL9A3collagen type IX alpha 3 chain | Zawsze | W 1 chorobie |
| CRNKL1crooked neck pre-mRNA splicing factor 1 | Zawsze | W 1 chorobie |
| EFEMP1EGF-like fibulin extracellular matrix protein 1 | Zawsze | W 1 chorobie |
| ERI1exoribonuclease 1 | Zawsze | W 1 chorobie |
| EXOSC5exosome component 5 | Zawsze | W 1 chorobie |
| FANCIFA complementation group I | Zawsze | W 2 chorobach |
| FBN1fibrillin 1 | Zawsze | W 3 chorobach |
| IFT172intraflagellar transport 172 | Zawsze | W 2 chorobach |
| INTS11integrator complex subunit 11 | Zawsze | W 1 chorobie |
| JKAMPJNK1/MAPK8 associated membrane protein | Zawsze | W 1 chorobie |
| KDM2Blysine demethylase 2B | Zawsze | W 1 chorobie |
| KDM6Blysine demethylase 6B | Zawsze | W 1 chorobie |
| LIG4DNA ligase 4 | Zawsze | W 1 chorobie |
| MAGmyelin associated glycoprotein | Zawsze | W 2 chorobach |
| MIR184microRNA 184 | Zawsze | W 1 chorobie |
| NR6A1nuclear receptor subfamily 6 group A member 1 | Zawsze | W 1 chorobie |
| PIGQphosphatidylinositol glycan anchor biosynthesis class Q | Zawsze | W 1 chorobie |
| REREarginine-glutamic acid dipeptide repeats | Zawsze | W 2 chorobach |
| SLC38A8solute carrier family 38 member 8 | Zawsze | W 1 chorobie |
| TUBTUB bipartite transcription factor | Zawsze | W 1 chorobie |
| UBAP2Lubiquitin associated protein 2 like | Zawsze | W 1 chorobie |
| AP3D1adaptor related protein complex 3 subunit delta 1 | Bardzo często (80–99%) | W 1 chorobie |
| DPYDdihydropyrimidine dehydrogenase | Bardzo często (80–99%) | W 2 chorobach |
| GPR143G protein-coupled receptor 143 | Bardzo często (80–99%) | W 2 chorobach |
| TCEAL1transcription elongation factor A like 1 | Bardzo często (80–99%) | W 1 chorobie |
| TCF4transcription factor 4 | Bardzo często (80–99%) | W 2 chorobach |
| ADAMTS2ADAM metallopeptidase with thrombospondin type 1 motif 2 | Często (30–79%) | W 1 chorobie |
| ADAMTSL2ADAMTS like 2 | Często (30–79%) | W 2 chorobach |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Często (30–79%) | W 1 chorobie |
| APC2APC regulator of Wnt signaling pathway 2 | Często (30–79%) | W 1 chorobie |
| BBS9Bardet-Biedl syndrome 9 | Często (30–79%) | W 2 chorobach |
| BLOC1S3biogenesis of lysosomal organelles complex 1 subunit 3 | Często (30–79%) | W 1 chorobie |
Pokaż jeszcze 181 genów
| Gen | Jak często występuje | Choroby |
|---|---|---|
| CAMTA1calmodulin binding transcription activator 1 | Często (30–79%) | W 1 chorobie |
| CCDC47coiled-coil domain containing 47 | Często (30–79%) | W 1 chorobie |
| CHMP1Acharged multivesicular body protein 1A | Często (30–79%) | W 1 chorobie |
| CHST14carbohydrate sulfotransferase 14 | Często (30–79%) | W 2 chorobach |
| DSEdermatan sulfate epimerase | Często (30–79%) | W 1 chorobie |
| EBF3EBF transcription factor 3 | Często (30–79%) | W 2 chorobach |
| HDAC4histone deacetylase 4 | Często (30–79%) | W 1 chorobie |
| HRASHRas proto-oncogene, GTPase | Często (30–79%) | W 1 chorobie |
| INTS1integrator complex subunit 1 | Często (30–79%) | W 1 chorobie |
| KAT6Alysine acetyltransferase 6A | Często (30–79%) | W 1 chorobie |
| KDM5Blysine demethylase 5B | Często (30–79%) | W 1 chorobie |
| KIDINS220kinase D interacting substrate 220 | Często (30–79%) | W 1 chorobie |
| KMT2Blysine methyltransferase 2B | Często (30–79%) | W 2 chorobach |
| LMX1BLIM homeobox transcription factor 1 beta | Często (30–79%) | W 1 chorobie |
| LRRC8Cleucine rich repeat containing 8 VRAC subunit C | Często (30–79%) | W 1 chorobie |
| MBD5methyl-CpG binding domain protein 5 | Często (30–79%) | W 1 chorobie |
| MED16mediator complex subunit 16 | Często (30–79%) | W 1 chorobie |
| MYO1Hmyosin IH | Często (30–79%) | W 1 chorobie |
| NEUROD2neuronal differentiation 2 | Często (30–79%) | W 1 chorobie |
| NFIXnuclear factor I X | Często (30–79%) | W 1 chorobie |
| NSD1nuclear receptor binding SET domain protein 1 | Często (30–79%) | W 1 chorobie |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Często (30–79%) | W 1 chorobie |
| POGZpogo transposable element derived with ZNF domain | Często (30–79%) | W 2 chorobach |
| POLR3GLRNA polymerase III subunit GL | Często (30–79%) | W 1 chorobie |
| PRDM5PR/SET domain 5 | Często (30–79%) | W 1 chorobie |
| PRMT7protein arginine methyltransferase 7 | Często (30–79%) | W 1 chorobie |
| RNF2ring finger protein 2 | Często (30–79%) | W 1 chorobie |
| RNU4-2RNA, U4 small nuclear 2 | Często (30–79%) | W 1 chorobie |
| RNU5B-1RNA, U5B small nuclear 1 | Często (30–79%) | W 1 chorobie |
| SETD5SET domain containing 5 | Często (30–79%) | W 1 chorobie |
| SLC25A24solute carrier family 25 member 24 | Często (30–79%) | W 1 chorobie |
| SLC2A10solute carrier family 2 member 10 | Często (30–79%) | W 1 chorobie |
| STXBP1syntaxin binding protein 1 | Często (30–79%) | W 1 chorobie |
| TGFBItransforming growth factor beta induced | Często (30–79%) | W 2 chorobach |
| WACWW domain containing adaptor with coiled-coil | Często (30–79%) | W 2 chorobach |
| ZNF469zinc finger protein 469 | Często (30–79%) | W 1 chorobie |
| AARS1alanyl-tRNA synthetase 1 | Czasami (5–29%) | W 1 chorobie |
| ADNPactivity dependent neuroprotector homeobox | Czasami (5–29%) | W 2 chorobach |
| AEBP1AE binding protein 1 | Czasami (5–29%) | W 1 chorobie |
| ANKRD11ankyrin repeat domain 11 | Czasami (5–29%) | W 1 chorobie |
| ARCN1archain 1 coat protein complex I subunit delta | Czasami (5–29%) | W 1 chorobie |
| ASH1LASH1 like histone lysine methyltransferase | Czasami (5–29%) | W 1 chorobie |
| BAP1BRCA1 associated deubiquitinase 1 | Czasami (5–29%) | W 1 chorobie |
| BBIP1BBSome interacting protein 1 | Czasami (5–29%) | W 1 chorobie |
| BBS10Bardet-Biedl syndrome 10 | Czasami (5–29%) | W 1 chorobie |
| BBS12Bardet-Biedl syndrome 12 | Czasami (5–29%) | W 1 chorobie |
| BBS2Bardet-Biedl syndrome 2 | Czasami (5–29%) | W 1 chorobie |
| BBS4Bardet-Biedl syndrome 4 | Czasami (5–29%) | W 1 chorobie |
| BBS5Bardet-Biedl syndrome 5 | Czasami (5–29%) | W 1 chorobie |
| BBS7Bardet-Biedl syndrome 7 | Czasami (5–29%) | W 1 chorobie |
| BRCA1BRCA1 DNA repair associated | Czasami (5–29%) | W 1 chorobie |
| BRCA2BRCA2 DNA repair associated | Czasami (5–29%) | W 1 chorobie |
| BRIP1BRCA1 interacting DNA helicase 1 | Czasami (5–29%) | W 1 chorobie |
| C1QBPcomplement C1q binding protein | Czasami (5–29%) | W 1 chorobie |
| CAMK2Bcalcium/calmodulin dependent protein kinase II beta | Czasami (5–29%) | W 1 chorobie |
| CAMSAP1calmodulin regulated spectrin associated protein 1 | Czasami (5–29%) | W 1 chorobie |
| CAPRIN1cell cycle associated protein 1 | Czasami (5–29%) | W 1 chorobie |
| CARS1cysteinyl-tRNA synthetase 1 | Czasami (5–29%) | W 1 chorobie |
| CEP19centrosomal protein 19 | Czasami (5–29%) | W 1 chorobie |
| CEP290centrosomal protein 290 | Czasami (5–29%) | W 1 chorobie |
| CFAP418cilia and flagella associated protein 418 | Czasami (5–29%) | W 1 chorobie |
| CHD3chromodomain helicase DNA binding protein 3 | Czasami (5–29%) | W 1 chorobie |
| CLDN16claudin 16 | Czasami (5–29%) | W 1 chorobie |
| COL4A5collagen type IV alpha 5 chain | Czasami (5–29%) | W 1 chorobie |
| COL8A2collagen type VIII alpha 2 chain | Czasami (5–29%) | W 1 chorobie |
| CRELD1CRELD disulfide isomerase 1 | Czasami (5–29%) | W 1 chorobie |
| DBR1debranching RNA lariats 1 | Czasami (5–29%) | W 1 chorobie |
| DPAGT1dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Czasami (5–29%) | W 1 chorobie |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Czasami (5–29%) | W 2 chorobach |
| EDEM3ER degradation enhancing alpha-mannosidase like protein 3 | Czasami (5–29%) | W 1 chorobie |
| EMC1ER membrane protein complex subunit 1 | Czasami (5–29%) | W 2 chorobach |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Czasami (5–29%) | W 1 chorobie |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Czasami (5–29%) | W 1 chorobie |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Czasami (5–29%) | W 2 chorobach |
| FAAP100FA core complex associated protein 100 | Czasami (5–29%) | W 1 chorobie |
| FANCAFA complementation group A | Czasami (5–29%) | W 1 chorobie |
| FANCBFA complementation group B | Czasami (5–29%) | W 1 chorobie |
| FANCCFA complementation group C | Czasami (5–29%) | W 1 chorobie |
| FANCD2FA complementation group D2 | Czasami (5–29%) | W 1 chorobie |
| FANCEFA complementation group E | Czasami (5–29%) | W 1 chorobie |
| FANCFFA complementation group F | Czasami (5–29%) | W 1 chorobie |
| FANCGFA complementation group G | Czasami (5–29%) | W 1 chorobie |
| FANCLFA complementation group L | Czasami (5–29%) | W 1 chorobie |
| FANCMFA complementation group M | Czasami (5–29%) | W 1 chorobie |
| FEM1Bfem-1 homolog B | Czasami (5–29%) | W 1 chorobie |
| FIBPFGF1 intracellular binding protein | Czasami (5–29%) | W 1 chorobie |
| FLNAfilamin A | Czasami (5–29%) | W 1 chorobie |
| GALNT2polypeptide N-acetylgalactosaminyltransferase 2 | Czasami (5–29%) | W 1 chorobie |
| GATAD2BGATA zinc finger domain containing 2B | Czasami (5–29%) | W 1 chorobie |
| GRHL2grainyhead like transcription factor 2 | Czasami (5–29%) | W 1 chorobie |
| GRIA1glutamate ionotropic receptor AMPA type subunit 1 | Czasami (5–29%) | W 1 chorobie |
| GTF2E2general transcription factor IIE subunit 2 | Czasami (5–29%) | W 1 chorobie |
| GTF2H5general transcription factor IIH subunit 5 | Czasami (5–29%) | W 1 chorobie |
| H1-4H1.4 linker histone, cluster member | Czasami (5–29%) | W 1 chorobie |
| HK1hexokinase 1 | Czasami (5–29%) | W 1 chorobie |
| IFT27intraflagellar transport 27 | Czasami (5–29%) | W 1 chorobie |
| IFT74intraflagellar transport 74 | Czasami (5–29%) | W 1 chorobie |
| KIF11kinesin family member 11 | Czasami (5–29%) | W 1 chorobie |
| KRASKRas proto-oncogene, GTPase | Czasami (5–29%) | W 1 chorobie |
| LMBRD2LMBR1 domain containing 2 | Czasami (5–29%) | W 1 chorobie |
| LTBP3latent transforming growth factor beta binding protein 3 | Czasami (5–29%) | W 1 chorobie |
| LZTFL1leucine zipper transcription factor like 1 | Czasami (5–29%) | W 1 chorobie |
| MAD2L2mitotic arrest deficient 2 like 2 | Czasami (5–29%) | W 1 chorobie |
| MAN2B1mannosidase alpha class 2B member 1 | Czasami (5–29%) | W 1 chorobie |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Czasami (5–29%) | W 1 chorobie |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Czasami (5–29%) | W 1 chorobie |
| MKKSMKKS centrosomal shuttling protein | Czasami (5–29%) | W 1 chorobie |
| MKS1MKS transition zone complex subunit 1 | Czasami (5–29%) | W 1 chorobie |
| MPLKIPM-phase specific PLK1 interacting protein | Czasami (5–29%) | W 1 chorobie |
| MYT1Lmyelin transcription factor 1 like | Czasami (5–29%) | W 1 chorobie |
| NOGnoggin | Czasami (5–29%) | W 1 chorobie |
| NOTCH3notch receptor 3 | Czasami (5–29%) | W 1 chorobie |
| NPHP1nephrocystin 1 | Czasami (5–29%) | W 1 chorobie |
| NRASNRAS proto-oncogene, GTPase | Czasami (5–29%) | W 1 chorobie |
| OTUD5OTU deubiquitinase 5 | Czasami (5–29%) | W 1 chorobie |
| OVOL2ovo like zinc finger 2 | Czasami (5–29%) | W 1 chorobie |
| PACS2phosphofurin acidic cluster sorting protein 2 | Czasami (5–29%) | W 1 chorobie |
| PALB2partner and localizer of BRCA2 | Czasami (5–29%) | W 1 chorobie |
| PAX2paired box 2 | Czasami (5–29%) | W 1 chorobie |
| PBX1PBX homeobox 1 | Czasami (5–29%) | W 1 chorobie |
| PDZD8PDZ domain containing 8 | Czasami (5–29%) | W 1 chorobie |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Czasami (5–29%) | W 1 chorobie |
| PPFIA3PPFI scaffold protein A3 | Czasami (5–29%) | W 1 chorobie |
| PPP1R12Aprotein phosphatase 1 regulatory subunit 12A | Czasami (5–29%) | W 1 chorobie |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | Czasami (5–29%) | W 1 chorobie |
| PTBP1polypyrimidine tract binding protein 1 | Czasami (5–29%) | W 1 chorobie |
| RAD51RAD51 recombinase | Czasami (5–29%) | W 1 chorobie |
| RAD51CRAD51 paralog C | Czasami (5–29%) | W 1 chorobie |
| RAP1BRAP1B, member of RAS oncogene family | Czasami (5–29%) | W 1 chorobie |
| RECQL4RecQ like helicase 4 | Czasami (5–29%) | W 1 chorobie |
| RFWD3ring finger and WD repeat domain 3 | Czasami (5–29%) | W 1 chorobie |
| RHOAras homolog family member A | Czasami (5–29%) | W 1 chorobie |
| RNF113Aring finger protein 113A | Czasami (5–29%) | W 1 chorobie |
| RNU4ATACRNA, U4atac small nuclear | Czasami (5–29%) | W 1 chorobie |
| SCAPERS-phase cyclin A associated protein in the ER | Czasami (5–29%) | W 1 chorobie |
| SCLT1sodium channel and clathrin linker 1 | Czasami (5–29%) | W 1 chorobie |
| SCUBE3signal peptide, CUB domain and EGF like domain containing 3 | Czasami (5–29%) | W 1 chorobie |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Czasami (5–29%) | W 1 chorobie |
| SETBP1SET binding protein 1 | Czasami (5–29%) | W 1 chorobie |
| SGSM3small G protein signaling modulator 3 | Czasami (5–29%) | W 1 chorobie |
| SHOC2SHOC2 leucine rich repeat scaffold protein | Czasami (5–29%) | W 1 chorobie |
| SLC39A8solute carrier family 39 member 8 | Czasami (5–29%) | W 2 chorobach |
| SLX4SLX4 structure-specific endonuclease subunit | Czasami (5–29%) | W 1 chorobie |
| SMG8SMG8 nonsense mediated mRNA decay factor | Czasami (5–29%) | W 1 chorobie |
| TARS1threonyl-tRNA synthetase 1 | Czasami (5–29%) | W 1 chorobie |
| TBC1D7TBC1 domain family member 7 | Czasami (5–29%) | W 1 chorobie |
| TBCEtubulin folding cofactor E | Czasami (5–29%) | W 1 chorobie |
| TNPO2transportin 2 | Czasami (5–29%) | W 1 chorobie |
| TRA2Btransformer 2 beta homolog | Czasami (5–29%) | W 1 chorobie |
| TRIM32tripartite motif containing 32 | Czasami (5–29%) | W 1 chorobie |
| TTC8tetratricopeptide repeat domain 8 | Czasami (5–29%) | W 1 chorobie |
| UBE2Tubiquitin conjugating enzyme E2 T | Czasami (5–29%) | W 1 chorobie |
| USP9Xubiquitin specific peptidase 9 X-linked | Czasami (5–29%) | W 2 chorobach |
| VSX1visual system homeobox 1 | Czasami (5–29%) | W 2 chorobach |
| WDPCPWD repeat containing planar cell polarity effector | Czasami (5–29%) | W 1 chorobie |
| XRCC2X-ray repair cross complementing 2 | Czasami (5–29%) | W 1 chorobie |
| YY1YY1 transcription factor | Czasami (5–29%) | W 1 chorobie |
| ZBTB7Azinc finger and BTB domain containing 7A | Czasami (5–29%) | W 1 chorobie |
| ZEB1zinc finger E-box binding homeobox 1 | Czasami (5–29%) | W 1 chorobie |
| ZEB2zinc finger E-box binding homeobox 2 | Czasami (5–29%) | W 2 chorobach |
| ZFXzinc finger protein X-linked | Czasami (5–29%) | W 1 chorobie |
| COL4A1collagen type IV alpha 1 chain | Rzadko (1–4%) | W 1 chorobie |
| FBXW7F-box and WD repeat domain containing 7 | Rzadko (1–4%) | W 1 chorobie |
| MARK2microtubule affinity regulating kinase 2 | Rzadko (1–4%) | W 1 chorobie |
| PPP2R5Dprotein phosphatase 2 regulatory subunit B'delta | Rzadko (1–4%) | W 1 chorobie |
| ARID1BAT-rich interaction domain 1B | Nie odnotowano | W 1 chorobie |
| CC2D2Acoiled-coil and C2 domain containing 2A | Nie odnotowano | W 1 chorobie |
| CHD4chromodomain helicase DNA binding protein 4 | Nie odnotowano | W 1 chorobie |
| CHRDL1chordin like 1 | Nie odnotowano | W 1 chorobie |
| CLDN19claudin 19 | Nie odnotowano | W 1 chorobie |
| DNAJC21DnaJ heat shock protein family (Hsp40) member C21 | Nie odnotowano | W 1 chorobie |
| GLRBglycine receptor beta | Nie odnotowano | W 1 chorobie |
| KCNV2potassium voltage-gated channel modifier subfamily V member 2 | Nie odnotowano | W 1 chorobie |
| NIPBLNIPBL cohesin loading factor | Nie odnotowano | W 1 chorobie |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Nie odnotowano | W 1 chorobie |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Nie odnotowano | W 1 chorobie |
| TEAD1TEA domain transcription factor 1 | Nie odnotowano | W 1 chorobie |
| TRIM37tripartite motif containing 37 | Nie odnotowano | W 1 chorobie |
| TYRtyrosinase | Nie odnotowano | W 1 chorobie |
| UBE3Bubiquitin protein ligase E3B | Nie odnotowano | W 1 chorobie |
| ZMIZ1zinc finger MIZ-type containing 1 | Nie odnotowano | W 1 chorobie |
Jak często występuje wśród osób z jedną z chorób związanych z tym genem, najczęściej spośród wszystkich, według danych Human Phenotype Ontology. Te strony opisują cechy i badania, na których się opierają; nie są diagnozą, a w sprawie objawów należy zwrócić się do lekarza lub doradcy genetycznego.
Cechy podrzędne
Cechy nadrzędne
Skąd pochodzą te dane
- Human Phenotype Ontology, wydanie 2026-09-01: cecha, jej nazwy, definicja oraz geny z nią powiązane. Więcej informacji znajdą Państwo na stronie hpo.jax.org.
- Wydanie danych 2026.10.16-c6eea6bf.
Jeden test. Odpowiedzi na całe życie.
Od 449 $Bezpłatna wysyłka · Wyniki w ciągu 6–8 tygodni