AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Özellik
Cat eye
Klinik adı: Iris coloboma
A coloboma of the iris.
Özet
- Diğer adları
- Coloboma of iris, Coloboma of the iris, Keyhole iris
- Vücut sistemi
- Abnormality of the eye
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Bu sayfanın veri olarak görünümü
Veriyi JSON olarak okumak için sayfa adresinin sonuna .json ekleyin veya application/json isteyin.
library(jsonlite)
url <- "https://dantelabs.com/traits/iris-coloboma.json"
page <- fromJSON(url)
page$trait$nameCat eyeHP:0000612
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
Cat eye ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi al58 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Joubert Syndrome And Related DisordersReads 34 of these genesCC2D2ACEP290INPP5ERPGRIP1LTMEM138TMEM216About this report →
- Congenital Muscular DystrophiesReads 13 of these genesB3GALNT2B4GAT1CRPPADAG1FKRPFKTNAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 12 of these genesBCORHMX1RBP4SHHBMP4FZD5About this report →
- Meckel SyndromeReads 7 of these genesRPGRIP1LTMEM231TMEM67B9D1B9D2MKS1About this report →
Show 54 more reports
- Treacher Collins SyndromeReads 4 of these genesPOLR1BPOLR1CPOLR1DTCOF1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 10 of these genesSHHOTX2SMOCDONDISP1GLI2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 12 of these genesCC2D2ACEP290TMEM138TMEM216TMEM231TMEM237About this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 2 of these genesPTCH1SUFUAbout this report →
- Congenital Disorders of GlycosylationReads 13 of these genesALG2PIGGSRD5A3CRPPADAG1FKRPAbout this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- Hajdu-Cheney SyndromeReads 1 of these genesNOTCH2About this report →
- Hereditary RetinoblastomaReads 1 of these genesRB1About this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- Hereditary Orofacial CleftingReads 2 of these genesBMP4TBX22About this report →
- Congenital Cranial Dysinnervation DisordersReads 2 of these genesCHN1MAFBAbout this report →
- Alagille SyndromeReads 1 of these genesNOTCH2About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Kabuki SyndromeReads 1 of these genesKMT2DAbout this report →
- Hypogonadotropic HypogonadismReads 5 of these genesCHD7FGFR1OTX2SMCHD1FGF8About this report →
- Limb-Girdle Muscular DystrophyReads 4 of these genesDAG1FKRPFKTNPOMGNT1About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 3 of these genesTMEM67ZNF423NPHP1About this report →
- Intellectual DisabilityReads 10 of these genesNAA10NSD2PIGGPOGZPUF60VPS13BAbout this report →
- Noonan SyndromeReads 3 of these genesHRASKRASNRASAbout this report →
- Bardet-Biedl and Alström SyndromesReads 3 of these genesCEP290IFT74MKS1About this report →
- Hereditary Congenital & Juvenile CataractReads 3 of these genesCRYBA4CRYBB1MAFAbout this report →
- Syndromic CraniosynostosisReads 3 of these genesFGFR1SMOFGFR2About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesKIFBPAbout this report →
- MedulloblastomaReads 1 of these genesSUFUAbout this report →
- Inherited ThrombocytopeniasReads 3 of these genesACTBFLI1RAP1BAbout this report →
- Retinitis PigmentosaReads 4 of these genesCC2D2AARL3OFD1POMGNT1About this report →
- Hereditary SpherocytosisReads 1 of these genesANK1About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Hypertrophic CardiomyopathyReads 3 of these genesHRASKRASNRASAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesELP4About this report →
- Kidney CancerReads 1 of these genesELP4About this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesNODALAbout this report →
- Epilepsy (Full Panel)Reads 4 of these genesCPLX1ATP6V1AFLNAZEB2About this report →
- Urinary and Renal System TumourReads 1 of these genesELP4About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Cutis LaxaReads 1 of these genesATP6V1AAbout this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesPNPLA6WASHC5About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGGAbout this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 1 of these genesCEP290About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR1CAbout this report →
- Congenital Myasthenic SyndromeReads 1 of these genesALG2About this report →
- VitreoretinopathyReads 1 of these genesATOH7About this report →
- Osteogenesis ImperfectaReads 1 of these genesMBTPS2About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesMBTPS2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesACTBAbout this report →
- Dilated CardiomyopathyReads 1 of these genesFKTNAbout this report →
- Primary Ciliary DyskinesiaReads 1 of these genesCENPFAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesPOLR1CAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesACTG1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesNDUFB11About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesKRASAbout this report →
Cat eye ile bağlantılı genleri ve genomunuzun geri kalanını tek bir testle okuyun.
$449'den başlayanÜcretsiz kargo · Sonuçlar 6–8 hafta içinde
Genome Test'imi alCat eye ile ilişkili 181 gen
Bu genlerdeki değişiklikler, Cat eye özelliğinin görüldüğü nadir durumlara yol açar. Bu özelliğe sahip çoğu kişide bu durumlardan hiçbiri yoktur; ayrıca bu listedeki bir gen, kimsenin kendi genomu hakkında bir şey söylemez.
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| ABCB6ATP binding cassette subfamily B member 6 (LAN blood group) | Her zaman | 1 durumda |
| ALG2ALG2 alpha-1,3/1,6-mannosyltransferase | Her zaman | 2 durumda |
| BCORBCL6 corepressor | Her zaman | 4 durumda |
| ESAMendothelial cell adhesion molecule | Her zaman | 1 durumda |
| HMGB3high mobility group box 3 | Her zaman | 1 durumda |
| HMX1H6 family homeobox 1 | Her zaman | 1 durumda |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Her zaman | 2 durumda |
| RBP4retinol binding protein 4 | Her zaman | 2 durumda |
| TENM3teneurin transmembrane protein 3 | Her zaman | 1 durumda |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Her zaman | 1 durumda |
| ACTBactin beta | Çok sık (%80–99) | 2 durumda |
| ACTG1actin gamma 1 | Çok sık (%80–99) | 1 durumda |
| CHD7chromodomain helicase DNA binding protein 7 | Çok sık (%80–99) | 2 durumda |
| HRASHRas proto-oncogene, GTPase | Çok sık (%80–99) | 1 durumda |
| KRASKRas proto-oncogene, GTPase | Çok sık (%80–99) | 2 durumda |
| NRASNRAS proto-oncogene, GTPase | Çok sık (%80–99) | 1 durumda |
| SEMA3Esemaphorin 3E | Çok sık (%80–99) | 1 durumda |
| SHHsonic hedgehog signaling molecule | Çok sık (%80–99) | 2 durumda |
| YAP1Yes1 associated transcriptional regulator | Çok sık (%80–99) | 2 durumda |
| ALX3ALX homeobox 3 | Sık (%30–79) | 1 durumda |
| BMP4bone morphogenetic protein 4 | Sık (%30–79) | 1 durumda |
| CC2D2Acoiled-coil and C2 domain containing 2A | Sık (%30–79) | 2 durumda |
| CEP290centrosomal protein 290 | Sık (%30–79) | 1 durumda |
| CPLX1complexin 1 | Sık (%30–79) | 2 durumda |
| CTBP1C-terminal binding protein 1 | Sık (%30–79) | 2 durumda |
| ELP4elongator acetyltransferase complex subunit 4 | Sık (%30–79) | 1 durumda |
| FGFR1fibroblast growth factor receptor 1 | Sık (%30–79) | 3 durumda |
| FGFRL1fibroblast growth factor receptor like 1 | Sık (%30–79) | 1 durumda |
| FZD5frizzled class receptor 5 | Sık (%30–79) | 1 durumda |
| GZF1GDNF inducible zinc finger protein 1 | Sık (%30–79) | 1 durumda |
| IGBP1immunoglobulin binding protein 1 | Sık (%30–79) | 2 durumda |
| INPP5Einositol polyphosphate-5-phosphatase E | Sık (%30–79) | 3 durumda |
| KIFBPkinesin family binding protein | Sık (%30–79) | 1 durumda |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Sık (%30–79) | 2 durumda |
| LRP2LDL receptor related protein 2 | Sık (%30–79) | 2 durumda |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Sık (%30–79) | 1 durumda |
| MIR204microRNA 204 | Sık (%30–79) | 1 durumda |
| NELFAnegative elongation factor complex member A | Sık (%30–79) | 1 durumda |
| NR6A1nuclear receptor subfamily 6 group A member 1 | Sık (%30–79) | 1 durumda |
| NSD2nuclear receptor binding SET domain protein 2 | Sık (%30–79) | 2 durumda |
141 gen daha göster
| Gen | Ne sıklıkla görüldüğü | Durumlar |
|---|---|---|
| OTX2orthodenticle homeobox 2 | Sık (%30–79) | 1 durumda |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Sık (%30–79) | 1 durumda |
| POGZpogo transposable element derived with ZNF domain | Sık (%30–79) | 2 durumda |
| POLR1BRNA polymerase I subunit B | Sık (%30–79) | 1 durumda |
| POLR1CRNA polymerase I and III subunit C | Sık (%30–79) | 1 durumda |
| POLR1DRNA polymerase I and III subunit D | Sık (%30–79) | 1 durumda |
| PORCNporcupine O-acyltransferase | Sık (%30–79) | 2 durumda |
| PRR12proline rich 12 | Sık (%30–79) | 1 durumda |
| RB1RB transcriptional corepressor 1 | Sık (%30–79) | 1 durumda |
| RBSNrabenosyn, RAB effector | Sık (%30–79) | 1 durumda |
| ROR1ROR family WNT receptor 1 | Sık (%30–79) | 1 durumda |
| RPGRIP1LRPGRIP1 like | Sık (%30–79) | 2 durumda |
| RSPO2R-spondin 2 | Sık (%30–79) | 1 durumda |
| SALL2spalt like transcription factor 2 | Sık (%30–79) | 1 durumda |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Sık (%30–79) | 1 durumda |
| SMOsmoothened, frizzled class receptor | Sık (%30–79) | 2 durumda |
| SRD5A3steroid 5 alpha-reductase 3 | Sık (%30–79) | 1 durumda |
| TBX22T-box transcription factor 22 | Sık (%30–79) | 1 durumda |
| TBX4T-box transcription factor 4 | Sık (%30–79) | 1 durumda |
| TCOF1treacle ribosome biogenesis factor 1 | Sık (%30–79) | 1 durumda |
| TFAP2Atranscription factor AP-2 alpha | Sık (%30–79) | 2 durumda |
| TMEM138transmembrane protein 138 | Sık (%30–79) | 1 durumda |
| TMEM216transmembrane protein 216 | Sık (%30–79) | 1 durumda |
| TMEM231transmembrane protein 231 | Sık (%30–79) | 1 durumda |
| TMEM237transmembrane protein 237 | Sık (%30–79) | 3 durumda |
| TMEM67transmembrane protein 67 | Sık (%30–79) | 2 durumda |
| WNT3Wnt family member 3 | Sık (%30–79) | 1 durumda |
| ZNF423zinc finger protein 423 | Sık (%30–79) | 1 durumda |
| AHI1Abelson helper integration site 1 | Bazen (%5–29) | 2 durumda |
| ANK1ankyrin 1 | Bazen (%5–29) | 1 durumda |
| ARL13BARF like GTPase 13B | Bazen (%5–29) | 1 durumda |
| ARL3ARF like GTPase 3 | Bazen (%5–29) | 1 durumda |
| ARMC9armadillo repeat containing 9 | Bazen (%5–29) | 1 durumda |
| ATOH7atonal bHLH transcription factor 7 | Bazen (%5–29) | 1 durumda |
| ATP6V1AATPase H+ transporting V1 subunit A | Bazen (%5–29) | 1 durumda |
| B3GALNT2beta-1,3-N-acetylgalactosaminyltransferase 2 | Bazen (%5–29) | 1 durumda |
| B4GAT1beta-1,4-glucuronyltransferase 1 | Bazen (%5–29) | 1 durumda |
| B9D1B9 domain containing 1 | Bazen (%5–29) | 1 durumda |
| B9D2B9 domain containing 2 | Bazen (%5–29) | 1 durumda |
| C12orf57chromosome 12 open reading frame 57 | Bazen (%5–29) | 1 durumda |
| CBY1chibby 1, beta catenin antagonist | Bazen (%5–29) | 1 durumda |
| CCDC22CCC complex scaffolding subunit CCDC22 | Bazen (%5–29) | 1 durumda |
| CDONcell adhesion associated, oncogene regulated | Bazen (%5–29) | 1 durumda |
| CEP104centrosomal protein 104 | Bazen (%5–29) | 1 durumda |
| CEP120centrosomal protein 120 | Bazen (%5–29) | 2 durumda |
| CEP41centrosomal protein 41 | Bazen (%5–29) | 2 durumda |
| CHN1chimerin 1 | Bazen (%5–29) | 1 durumda |
| COL4A1collagen type IV alpha 1 chain | Bazen (%5–29) | 1 durumda |
| CPLANE1ciliogenesis and planar polarity effector complex subunit 1 | Bazen (%5–29) | 1 durumda |
| CRIPTOcripto, EGF-CFC family member | Bazen (%5–29) | 1 durumda |
| CRPPACDP-L-ribitol pyrophosphorylase A | Bazen (%5–29) | 1 durumda |
| CRYAAcrystallin alpha A | Bazen (%5–29) | 2 durumda |
| CRYBA4crystallin beta A4 | Bazen (%5–29) | 1 durumda |
| CRYBB1crystallin beta B1 | Bazen (%5–29) | 1 durumda |
| CRYBB2crystallin beta B2 | Bazen (%5–29) | 1 durumda |
| CRYGCcrystallin gamma C | Bazen (%5–29) | 1 durumda |
| CRYGDcrystallin gamma D | Bazen (%5–29) | 1 durumda |
| CSPP1centrosome and spindle pole associated protein 1 | Bazen (%5–29) | 1 durumda |
| DACT1dishevelled binding antagonist of beta catenin 1 | Bazen (%5–29) | 1 durumda |
| DAG1dystroglycan 1 | Bazen (%5–29) | 1 durumda |
| DHCR77-dehydrocholesterol reductase | Bazen (%5–29) | 1 durumda |
| DISP1dispatched RND transporter family member 1 | Bazen (%5–29) | 1 durumda |
| DLL1delta like canonical Notch ligand 1 | Bazen (%5–29) | 1 durumda |
| DPYSL5dihydropyrimidinase like 5 | Bazen (%5–29) | 1 durumda |
| FGF3fibroblast growth factor 3 | Bazen (%5–29) | 1 durumda |
| FGF8fibroblast growth factor 8 | Bazen (%5–29) | 1 durumda |
| FGFR2fibroblast growth factor receptor 2 | Bazen (%5–29) | 1 durumda |
| FKRPfukutin related protein | Bazen (%5–29) | 1 durumda |
| FKTNfukutin | Bazen (%5–29) | 1 durumda |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Bazen (%5–29) | 1 durumda |
| FLNAfilamin A | Bazen (%5–29) | 2 durumda |
| FOXH1forkhead box H1 | Bazen (%5–29) | 1 durumda |
| GAS1growth arrest specific 1 | Bazen (%5–29) | 1 durumda |
| GJA8gap junction protein alpha 8 | Bazen (%5–29) | 1 durumda |
| GLI2GLI family zinc finger 2 | Bazen (%5–29) | 1 durumda |
| GNAQG protein subunit alpha q | Bazen (%5–29) | 1 durumda |
| HYLS1HYLS1 centriolar and ciliogenesis associated | Bazen (%5–29) | 1 durumda |
| IFT74intraflagellar transport 74 | Bazen (%5–29) | 1 durumda |
| KATNIPkatanin interacting protein | Bazen (%5–29) | 1 durumda |
| KCTD1potassium channel tetramerization domain containing 1 | Bazen (%5–29) | 1 durumda |
| KIAA0586KIAA0586 | Bazen (%5–29) | 1 durumda |
| KIAA0753KIAA0753 | Bazen (%5–29) | 1 durumda |
| KMT2Dlysine methyltransferase 2D | Bazen (%5–29) | 1 durumda |
| LARGE1LARGE xylosyl- and glucuronyltransferase 1 | Bazen (%5–29) | 1 durumda |
| MAFMAF bZIP transcription factor | Bazen (%5–29) | 2 durumda |
| MAFBMAF bZIP transcription factor B | Bazen (%5–29) | 1 durumda |
| MED12Lmediator complex subunit 12L | Bazen (%5–29) | 1 durumda |
| MKS1MKS transition zone complex subunit 1 | Bazen (%5–29) | 3 durumda |
| MMP14matrix metallopeptidase 14 | Bazen (%5–29) | 1 durumda |
| MMP2matrix metallopeptidase 2 | Bazen (%5–29) | 1 durumda |
| NODALnodal growth differentiation factor | Bazen (%5–29) | 1 durumda |
| NOTCH2notch receptor 2 | Bazen (%5–29) | 2 durumda |
| NOTCH3notch receptor 3 | Bazen (%5–29) | 1 durumda |
| NPHP1nephrocystin 1 | Bazen (%5–29) | 1 durumda |
| OFD1OFD1 centriole and centriolar satellite protein | Bazen (%5–29) | 1 durumda |
| PDE6Dphosphodiesterase 6D | Bazen (%5–29) | 1 durumda |
| PIBF1progesterone immunomodulatory binding factor 1 | Bazen (%5–29) | 1 durumda |
| PNPLA6patatin like domain 6, lysophospholipase | Bazen (%5–29) | 1 durumda |
| POMGNT1protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Bazen (%5–29) | 1 durumda |
| POMGNT2protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) | Bazen (%5–29) | 1 durumda |
| POMKprotein O-mannose kinase | Bazen (%5–29) | 1 durumda |
| POMT1protein O-mannosyltransferase 1 | Bazen (%5–29) | 1 durumda |
| POMT2protein O-mannosyltransferase 2 | Bazen (%5–29) | 1 durumda |
| PTCH1patched 1 | Bazen (%5–29) | 4 durumda |
| PTCH2patched 2 | Bazen (%5–29) | 1 durumda |
| PUF60poly(U) binding splicing factor 60 | Bazen (%5–29) | 1 durumda |
| RAP1BRAP1B, member of RAS oncogene family | Bazen (%5–29) | 1 durumda |
| REREarginine-glutamic acid dipeptide repeats | Bazen (%5–29) | 1 durumda |
| RXYLT1ribitol xylosyltransferase 1 | Bazen (%5–29) | 1 durumda |
| SALL1spalt like transcription factor 1 | Bazen (%5–29) | 1 durumda |
| SALL4spalt like transcription factor 4 | Bazen (%5–29) | 3 durumda |
| SIX3SIX homeobox 3 | Bazen (%5–29) | 2 durumda |
| SIX6SIX homeobox 6 | Bazen (%5–29) | 1 durumda |
| SOX2SRY-box transcription factor 2 | Bazen (%5–29) | 1 durumda |
| SUFUSUFU negative regulator of hedgehog signaling | Bazen (%5–29) | 3 durumda |
| TCEAL1transcription elongation factor A like 1 | Bazen (%5–29) | 1 durumda |
| TCTN1tectonic family member 1 | Bazen (%5–29) | 1 durumda |
| TCTN2tectonic family member 2 | Bazen (%5–29) | 1 durumda |
| TCTN3tectonic family member 3 | Bazen (%5–29) | 1 durumda |
| TGIF1TGFB induced factor homeobox 1 | Bazen (%5–29) | 1 durumda |
| TMEM218transmembrane protein 218 | Bazen (%5–29) | 1 durumda |
| TOGARAM1TOG array regulator of axonemal microtubules 1 | Bazen (%5–29) | 1 durumda |
| VPS13Bvacuolar protein sorting 13 homolog B | Bazen (%5–29) | 1 durumda |
| VPS35LVPS35 endosomal protein sorting factor like | Bazen (%5–29) | 1 durumda |
| WASHC5WASH complex subunit 5 | Bazen (%5–29) | 1 durumda |
| ZEB2zinc finger E-box binding homeobox 2 | Bazen (%5–29) | 3 durumda |
| ZIC2Zic family zinc finger 2 | Bazen (%5–29) | 1 durumda |
| ADNPactivity dependent neuroprotector homeobox | Seyrek (%1–4) | 1 durumda |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Seyrek (%1–4) | 1 durumda |
| SIN3ASIN3 transcription regulator family member A | Seyrek (%1–4) | 1 durumda |
| SPTBN1spectrin beta, non-erythrocytic 1 | Seyrek (%1–4) | 1 durumda |
| TRIM37tripartite motif containing 37 | Seyrek (%1–4) | 1 durumda |
| ALG3ALG3 alpha-1,3- mannosyltransferase | Kaydedilmedi | 1 durumda |
| B3GLCTbeta 3-glucosyltransferase | Kaydedilmedi | 1 durumda |
| CENPFcentromere protein F | Kaydedilmedi | 1 durumda |
| COX7Bcytochrome c oxidase subunit 7B | Kaydedilmedi | 1 durumda |
| GDF3growth differentiation factor 3 | Kaydedilmedi | 1 durumda |
| HCCSholocytochrome c synthase | Kaydedilmedi | 1 durumda |
| MPDZmultiple PDZ domain crumbs cell polarity complex component | Kaydedilmedi | 1 durumda |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Kaydedilmedi | 1 durumda |
| VSX2visual system homeobox 2 | Kaydedilmedi | 1 durumda |
Bu özelliğin, genin ilişkili olduğu durumlardan birine sahip kişiler arasında ne sıklıkta görüldüğü; Human Phenotype Ontology'nin kaydettiği şekliyle, bunlar arasında en sık görülen oran. Bu sayfalar özellikleri ve bunların arkasındaki araştırmaları anlatır; tanı koymaz. Belirtiler hakkında bir doktora veya genetik danışmana başvurmanız gerekir.
Daha geniş özellikler
Bilgilerin kaynağı
- Human Phenotype Ontology, 2026-09-01 sürümü: özellik, adları, tanımı ve buna bağlı genler. Ayrıntılar için hpo.jax.org adresine bakın.
- Veri sürümü 2026.10.18-e609d43e.
AtlasKimlere Yardımcı OluyoruzBilimimizÜrünlerSonuçlar
Giriş YapSorGenomunuzu dizileyin↗
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$449'den başlayan
Ücretsiz kargo · Sonuçlar 6–8 hafta içinde
