Cecha
Inward turning cross eyed
Nazwa kliniczna: Esotropia
A form of strabismus with one or both eyes turned inward ('crossed') to a relatively severe degree, usually defined as 10 diopters or more.
Podsumowanie
- 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 Inward turning cross eyed, and the rest of your genome, with one test.
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Zamawiam Genome Test204 genów powiązanych z Inward turning cross eyed
Zmiany w tych genach powodują rzadkie choroby, w których występuje Inward turning cross eyed. 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 |
|---|---|---|
| ADGRG1adhesion G protein-coupled receptor G1 | Zawsze | W 2 chorobach |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Zawsze | W 2 chorobach |
| ATIC5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase | Zawsze | W 1 chorobie |
| ATOH7atonal bHLH transcription factor 7 | Zawsze | W 1 chorobie |
| EBPEBP cholestenol delta-isomerase | Zawsze | W 1 chorobie |
| EXOSC5exosome component 5 | Zawsze | W 1 chorobie |
| FASTKD5FASTK mitochondrial RNA regulator 5 | Zawsze | W 1 chorobie |
| FBXO28F-box protein 28 | Zawsze | W 1 chorobie |
| FDXRferredoxin reductase | Zawsze | W 1 chorobie |
| H4C11H4 clustered histone 11 | Zawsze | W 1 chorobie |
| HMGB3high mobility group box 3 | Zawsze | W 1 chorobie |
| HOXB1homeobox B1 | Zawsze | W 1 chorobie |
| HPS3HPS3 biogenesis of lysosomal organelles complex 2 subunit 1 | Zawsze | W 1 chorobie |
| INPP4Ainositol polyphosphate-4-phosphatase type I A | Zawsze | W 1 chorobie |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Zawsze | W 1 chorobie |
| LGI4leucine rich repeat LGI family member 4 | Zawsze | W 1 chorobie |
| MED16mediator complex subunit 16 | Zawsze | W 1 chorobie |
| MYOD1myogenic differentiation 1 | Zawsze | W 1 chorobie |
| NHEJ1non-homologous end joining factor 1 | Zawsze | W 1 chorobie |
| NSD1nuclear receptor binding SET domain protein 1 | Zawsze | W 1 chorobie |
| POLGDNA polymerase gamma, catalytic subunit | Zawsze | W 1 chorobie |
| THAP11THAP domain containing 11 | Zawsze | W 1 chorobie |
| UBAP2Lubiquitin associated protein 2 like | Zawsze | W 1 chorobie |
| UNC13Aunc-13 homolog A | Zawsze | W 1 chorobie |
| ADAT3adenosine deaminase tRNA specific 3 | Bardzo często (80–99%) | W 1 chorobie |
| DDOSTdolichyl-diphosphooligosaccharide--protein glycosyltransferase non-catalytic subunit | Bardzo często (80–99%) | W 1 chorobie |
| SOBPsine oculis binding protein homolog | Bardzo często (80–99%) | W 1 chorobie |
| AHCYadenosylhomocysteinase | Często (30–79%) | W 1 chorobie |
| AHDC1AT-hook DNA binding motif containing 1 | Często (30–79%) | W 2 chorobach |
| ALG2ALG2 alpha-1,3/1,6-mannosyltransferase | Często (30–79%) | W 1 chorobie |
| ANTXR1ANTXR cell adhesion molecule 1 | Często (30–79%) | W 1 chorobie |
| ATAD3AATPase family AAA domain containing 3A | Często (30–79%) | W 2 chorobach |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Często (30–79%) | W 1 chorobie |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | Często (30–79%) | W 1 chorobie |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | Często (30–79%) | W 2 chorobach |
| CHMP1Acharged multivesicular body protein 1A | Często (30–79%) | W 1 chorobie |
| COL12A1collagen type XII alpha 1 chain | Często (30–79%) | W 1 chorobie |
| COL4A2collagen type IV alpha 2 chain | Często (30–79%) | W 1 chorobie |
| COL6A1collagen type VI alpha 1 chain | Często (30–79%) | W 1 chorobie |
| COL6A2collagen type VI alpha 2 chain | Często (30–79%) | W 1 chorobie |
Pokaż jeszcze 164 genów
| Gen | Jak często występuje | Choroby |
|---|---|---|
| COL6A3collagen type VI alpha 3 chain | Często (30–79%) | W 1 chorobie |
| CPLANE1ciliogenesis and planar polarity effector complex subunit 1 | Często (30–79%) | W 2 chorobach |
| EXOSC9exosome component 9 | Często (30–79%) | W 2 chorobach |
| FAM149B1family with sequence similarity 149 member B1 | Często (30–79%) | W 1 chorobie |
| FGF10fibroblast growth factor 10 | Często (30–79%) | W 1 chorobie |
| FZD4frizzled class receptor 4 | Często (30–79%) | W 1 chorobie |
| GALCgalactosylceramidase | Często (30–79%) | W 1 chorobie |
| GLRBglycine receptor beta | Często (30–79%) | W 1 chorobie |
| GRID2glutamate ionotropic receptor delta type subunit 2 | Często (30–79%) | W 1 chorobie |
| GRM1glutamate metabotropic receptor 1 | Często (30–79%) | W 2 chorobach |
| KAT6Alysine acetyltransferase 6A | Często (30–79%) | W 1 chorobie |
| KIAA0753KIAA0753 | Często (30–79%) | W 2 chorobach |
| KIDINS220kinase D interacting substrate 220 | Często (30–79%) | W 1 chorobie |
| KIF7kinesin family member 7 | Często (30–79%) | W 1 chorobie |
| LRP5LDL receptor related protein 5 | Często (30–79%) | W 1 chorobie |
| MAU2MAU2 sister chromatid cohesion factor | Często (30–79%) | W 1 chorobie |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Często (30–79%) | W 1 chorobie |
| NCDNneurochondrin | Często (30–79%) | W 1 chorobie |
| NEUROD2neuronal differentiation 2 | Często (30–79%) | W 1 chorobie |
| NEXMIFneurite extension and migration factor | Często (30–79%) | W 2 chorobach |
| OFD1OFD1 centriole and centriolar satellite protein | Często (30–79%) | W 1 chorobie |
| PDE6Dphosphodiesterase 6D | Często (30–79%) | W 1 chorobie |
| PHGDHphosphoglycerate dehydrogenase | Często (30–79%) | W 1 chorobie |
| PMM2phosphomannomutase 2 | Często (30–79%) | W 2 chorobach |
| POU4F1POU class 4 homeobox 1 | Często (30–79%) | W 1 chorobie |
| PPFIA3PPFI scaffold protein A3 | Często (30–79%) | W 1 chorobie |
| PPP1R21protein phosphatase 1 regulatory subunit 21 | Często (30–79%) | W 1 chorobie |
| RHOBTB2Rho related BTB domain containing 2 | Często (30–79%) | W 1 chorobie |
| ROBO3roundabout guidance receptor 3 | Często (30–79%) | W 1 chorobie |
| SALL2spalt like transcription factor 2 | Często (30–79%) | W 1 chorobie |
| SCN2Asodium voltage-gated channel alpha subunit 2 | Często (30–79%) | W 1 chorobie |
| SLC12A6solute carrier family 12 member 6 | Często (30–79%) | W 1 chorobie |
| SLC1A3solute carrier family 1 member 3 | Często (30–79%) | W 1 chorobie |
| SLC2A1solute carrier family 2 member 1 | Często (30–79%) | W 1 chorobie |
| SYT1synaptotagmin 1 | Często (30–79%) | W 1 chorobie |
| TCTN3tectonic family member 3 | Często (30–79%) | W 1 chorobie |
| TMEM216transmembrane protein 216 | Często (30–79%) | W 2 chorobach |
| TMEM231transmembrane protein 231 | Często (30–79%) | W 1 chorobie |
| TOPORSTOP1 binding arginine/serine rich protein, E3 ubiquitin ligase | Często (30–79%) | W 1 chorobie |
| TUBB3tubulin beta 3 class III | Często (30–79%) | W 2 chorobach |
| UNC80unc-80 subunit of NALCN channel complex | Często (30–79%) | W 1 chorobie |
| USP7ubiquitin specific peptidase 7 | Często (30–79%) | W 1 chorobie |
| ZSWIM6zinc finger SWIM-type containing 6 | Często (30–79%) | W 1 chorobie |
| AARS1alanyl-tRNA synthetase 1 | Czasami (5–29%) | W 1 chorobie |
| ABCC9ATP binding cassette subfamily C member 9 | Czasami (5–29%) | W 1 chorobie |
| AP1G1adaptor related protein complex 1 subunit gamma 1 | Czasami (5–29%) | W 1 chorobie |
| BLOC1S3biogenesis of lysosomal organelles complex 1 subunit 3 | Czasami (5–29%) | W 1 chorobie |
| CAMK2Bcalcium/calmodulin dependent protein kinase II beta | Czasami (5–29%) | W 1 chorobie |
| CARS1cysteinyl-tRNA synthetase 1 | Czasami (5–29%) | W 1 chorobie |
| CDKL5cyclin dependent kinase like 5 | Czasami (5–29%) | W 1 chorobie |
| CHD8chromodomain helicase DNA binding protein 8 | Czasami (5–29%) | W 1 chorobie |
| CLCN3Cl-/H+ antiporter 3 | Czasami (5–29%) | W 1 chorobie |
| COL25A1collagen type XXV alpha 1 chain | Czasami (5–29%) | W 1 chorobie |
| CRELD1CRELD disulfide isomerase 1 | Czasami (5–29%) | W 1 chorobie |
| CYB5Acytochrome b5 type A | Czasami (5–29%) | W 1 chorobie |
| CYB5R3cytochrome b5 reductase 3 | Czasami (5–29%) | W 1 chorobie |
| DBR1debranching RNA lariats 1 | Czasami (5–29%) | W 1 chorobie |
| DLK1delta like non-canonical Notch ligand 1 | Czasami (5–29%) | W 1 chorobie |
| DPM1dolichyl-phosphate mannosyltransferase subunit 1, catalytic | Czasami (5–29%) | W 1 chorobie |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | 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 |
| FAM177A1family with sequence similarity 177 member A1 | Czasami (5–29%) | W 1 chorobie |
| FRMD5FERM domain containing 5 | Czasami (5–29%) | W 1 chorobie |
| GNA14G protein subunit alpha 14 | Czasami (5–29%) | W 1 chorobie |
| GNB1G protein subunit beta 1 | Czasami (5–29%) | W 1 chorobie |
| GTF2E2general transcription factor IIE subunit 2 | Czasami (5–29%) | W 2 chorobach |
| GTF2H5general transcription factor IIH subunit 5 | Czasami (5–29%) | W 1 chorobie |
| GTF3C3general transcription factor IIIC subunit 3 | Czasami (5–29%) | W 1 chorobie |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Czasami (5–29%) | W 1 chorobie |
| HPDL4-hydroxyphenylpyruvate dioxygenase like | Czasami (5–29%) | W 1 chorobie |
| IRF2BPLinterferon regulatory factor 2 binding protein like | Czasami (5–29%) | W 1 chorobie |
| KAT8lysine acetyltransferase 8 | Czasami (5–29%) | W 1 chorobie |
| KCNMA1potassium calcium-activated channel subfamily M alpha 1 | Czasami (5–29%) | W 1 chorobie |
| KDM6Blysine demethylase 6B | Czasami (5–29%) | W 1 chorobie |
| KIF21Akinesin family member 21A | Czasami (5–29%) | W 2 chorobach |
| LIM2lens intrinsic membrane protein 2 | Czasami (5–29%) | W 1 chorobie |
| LRMDAleucine rich melanocyte differentiation associated | Czasami (5–29%) | W 1 chorobie |
| LRPPRCleucine rich pentatricopeptide repeat containing | Czasami (5–29%) | W 1 chorobie |
| LRRC7leucine rich repeat containing 7 | Czasami (5–29%) | W 1 chorobie |
| MADDMAP kinase activating death domain | Czasami (5–29%) | W 1 chorobie |
| MAGEL2MAGE family member L2 | Czasami (5–29%) | W 3 chorobach |
| MEG3maternally expressed 3 | Czasami (5–29%) | W 1 chorobie |
| MKRN3makorin ring finger protein 3 | Czasami (5–29%) | W 1 chorobie |
| MPLKIPM-phase specific PLK1 interacting protein | Czasami (5–29%) | W 1 chorobie |
| NALCNsodium leak channel, non-selective | Czasami (5–29%) | W 2 chorobach |
| NPAP1nuclear pore associated protein 1 | Czasami (5–29%) | W 1 chorobie |
| NR2F1nuclear receptor subfamily 2 group F member 1 | Czasami (5–29%) | W 1 chorobie |
| NTNG2netrin G2 | Czasami (5–29%) | W 1 chorobie |
| PCDHGC4protocadherin gamma subfamily C, 4 | Czasami (5–29%) | W 1 chorobie |
| PDE4Dphosphodiesterase 4D | Czasami (5–29%) | W 1 chorobie |
| PGAP2post-GPI attachment to proteins 2 | Czasami (5–29%) | W 1 chorobie |
| PGAP3post-GPI attachment to proteins phospholipase 3 | Czasami (5–29%) | W 1 chorobie |
| PHOX2Apaired like homeobox 2A | Czasami (5–29%) | W 1 chorobie |
| PIDD1p53-induced death domain protein 1 | Czasami (5–29%) | W 1 chorobie |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Czasami (5–29%) | W 1 chorobie |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Czasami (5–29%) | W 1 chorobie |
| PIGOphosphatidylinositol glycan anchor biosynthesis class O | Czasami (5–29%) | W 1 chorobie |
| PIGVphosphatidylinositol glycan anchor biosynthesis class V | Czasami (5–29%) | W 1 chorobie |
| PIGWphosphatidylinositol glycan anchor biosynthesis class W | Czasami (5–29%) | W 1 chorobie |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Czasami (5–29%) | W 1 chorobie |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Czasami (5–29%) | W 1 chorobie |
| POLA1DNA polymerase alpha 1, catalytic subunit | Czasami (5–29%) | W 1 chorobie |
| PORCNporcupine O-acyltransferase | Czasami (5–29%) | W 1 chorobie |
| PPP2R5Cprotein phosphatase 2 regulatory subunit B'gamma | Czasami (5–29%) | W 1 chorobie |
| PRKAR1Bprotein kinase cAMP-dependent type I regulatory subunit beta | Czasami (5–29%) | W 1 chorobie |
| PUF60poly(U) binding splicing factor 60 | Czasami (5–29%) | W 1 chorobie |
| PURApurine rich element binding protein A | Czasami (5–29%) | W 1 chorobie |
| PWAR1Prader Willi/Angelman region RNA 1 | Czasami (5–29%) | W 1 chorobie |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Czasami (5–29%) | W 1 chorobie |
| PYCR2pyrroline-5-carboxylate reductase 2 | Czasami (5–29%) | W 1 chorobie |
| REREarginine-glutamic acid dipeptide repeats | Czasami (5–29%) | W 1 chorobie |
| RNASEH1ribonuclease H1 | Czasami (5–29%) | W 1 chorobie |
| RNF113Aring finger protein 113A | Czasami (5–29%) | W 1 chorobie |
| RORARAR related orphan receptor A | Czasami (5–29%) | W 1 chorobie |
| RRAS2RAS related 2 | Czasami (5–29%) | W 1 chorobie |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Czasami (5–29%) | W 1 chorobie |
| RTL1retrotransposon Gag like 1 | Czasami (5–29%) | W 1 chorobie |
| SEC23ASEC23 homolog A, COPII component | Czasami (5–29%) | W 1 chorobie |
| SIAH1siah E3 ubiquitin protein ligase 1 | Czasami (5–29%) | W 1 chorobie |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Czasami (5–29%) | W 1 chorobie |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Czasami (5–29%) | W 1 chorobie |
| SONSON DNA and RNA binding protein | Czasami (5–29%) | W 1 chorobie |
| TARS1threonyl-tRNA synthetase 1 | Czasami (5–29%) | W 1 chorobie |
| TBCKTBC1 domain containing kinase | Czasami (5–29%) | W 1 chorobie |
| TTI1TELO2 interacting protein 1 | Czasami (5–29%) | W 1 chorobie |
| TUBA1Atubulin alpha 1a | Czasami (5–29%) | W 1 chorobie |
| TUBB2Btubulin beta 2B class IIb | Czasami (5–29%) | W 1 chorobie |
| UFC1ubiquitin-fold modifier conjugating enzyme 1 | Czasami (5–29%) | W 1 chorobie |
| UFSP2UFM1 specific peptidase 2 | Czasami (5–29%) | W 1 chorobie |
| WSB2WD repeat and SOCS box containing 2 | Czasami (5–29%) | W 1 chorobie |
| AGTPBP1ATP/GTP binding carboxypeptidase 1 | Rzadko (1–4%) | W 1 chorobie |
| COL8A2collagen type VIII alpha 2 chain | Rzadko (1–4%) | W 1 chorobie |
| EXOSC3exosome component 3 | Rzadko (1–4%) | W 1 chorobie |
| EXOSC8exosome component 8 | Rzadko (1–4%) | W 1 chorobie |
| FBN1fibrillin 1 | Rzadko (1–4%) | W 1 chorobie |
| GRHL2grainyhead like transcription factor 2 | Rzadko (1–4%) | W 1 chorobie |
| OVOL2ovo like zinc finger 2 | Rzadko (1–4%) | W 1 chorobie |
| SLC25A46solute carrier family 25 member 46 | Rzadko (1–4%) | W 1 chorobie |
| VRK1VRK serine/threonine kinase 1 | Rzadko (1–4%) | W 1 chorobie |
| VSX1visual system homeobox 1 | Rzadko (1–4%) | W 1 chorobie |
| ZEB1zinc finger E-box binding homeobox 1 | Rzadko (1–4%) | W 1 chorobie |
| AMMECR1AMMECR nuclear protein 1 | Nie odnotowano | W 1 chorobie |
| ARHGAP31Rho GTPase activating protein 31 | Nie odnotowano | W 1 chorobie |
| B3GAT3beta-1,3-glucuronyltransferase 3 | Nie odnotowano | W 1 chorobie |
| CHST3carbohydrate sulfotransferase 3 | Nie odnotowano | W 1 chorobie |
| CLP1cleavage factor polyribonucleotide kinase subunit 1 | Nie odnotowano | W 1 chorobie |
| COL11A1collagen type XI alpha 1 chain | Nie odnotowano | W 1 chorobie |
| CRB1crumbs cell polarity complex component 1 | Nie odnotowano | W 1 chorobie |
| GBA1glucosylceramidase beta 1 | Nie odnotowano | W 1 chorobie |
| HUWE1HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1 | Nie odnotowano | W 1 chorobie |
| IARS2isoleucyl-tRNA synthetase 2, mitochondrial | Nie odnotowano | W 1 chorobie |
| LAGE3L antigen family member 3 | Nie odnotowano | W 1 chorobie |
| MBD5methyl-CpG binding domain protein 5 | Nie odnotowano | W 1 chorobie |
| PEX5peroxisomal biogenesis factor 5 | Nie odnotowano | W 1 chorobie |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Nie odnotowano | W 1 chorobie |
| SOSTsclerostin | Nie odnotowano | W 1 chorobie |
| SREBF1sterol regulatory element binding transcription factor 1 | Nie odnotowano | W 1 chorobie |
| TBC1D23TBC1 domain family member 23 | Nie odnotowano | W 1 chorobie |
| TBX1T-box transcription factor 1 | Nie odnotowano | W 1 chorobie |
| TENM3teneurin transmembrane protein 3 | Nie odnotowano | W 1 chorobie |
| TRIT1tRNA isopentenyltransferase 1 | Nie odnotowano | W 1 chorobie |
| ZEB2zinc finger E-box binding homeobox 2 | 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