Tulajdonság
High levels of amniotic fluid
Klinikai név: Polyhydramnios
The presence of excess amniotic fluid in the uterus during pregnancy.
Összefoglaló
- Más néven
- Hydramnios
- Szervrendszer
- Abnormality of prenatal development or birth
Ez az oldal adatként
Adja hozzá a .json végződést az oldal címéhez, vagy kérjen application/json típust, hogy JSON-ként olvassa be.
library(jsonlite)
url <- "https://dantelabs.com/traits/polyhydramnios.json"
page <- fromJSON(url)
page$trait$nameOlvassa el a(z) High levels of amniotic fluid nevű génhez kapcsolódó információkat, valamint a genomja többi részét egyetlen teszttel.
449 $-tólIngyenes szállítás · Eredmények 6–8 hét alatt
Kérem a Genome Testemet130 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.
- Congenital MyopathiesReads 16 of these genesDNM2ACTA1BIN1KLHL40KLHL41LMOD3About this report →
- Noonan SyndromeReads 16 of these genesPPP1CBSOS1ERFHRASKRASLZTR1About this report →
- Hypertrophic CardiomyopathyReads 18 of these genesPPP1CBSOS1ERFHRASKRASLZTR1About this report →
- Bartter DiseaseReads 5 of these genesSLC12A1BSNDCLCNKBKCNJ1MAGED2About this report →
Show 126 more reports
- Congenital Myasthenic SyndromeReads 9 of these genesSCN4AMUSKPLECALG14DOK7RAPSNAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 4 of these genesACTG2MYH11MYLKERBB3About this report →
- Achondrogenesis panelReads 3 of these genesCOL2A1SLC26A2TRIP11About this report →
- Kabuki SyndromeReads 2 of these genesKDM6AKMT2DAbout this report →
- Nephrogenic Diabetes InsipidusReads 2 of these genesAQP2AVPR2About this report →
- Severe Inherited Insulin ResistanceReads 2 of these genesINSRAKT2About this report →
- Mosaic Variegated Aneuploidy SyndromeReads 3 of these genesBUB1BCEP57TRIP13About this report →
- Congenital Disorders of GlycosylationReads 13 of these genesB3GALT6PIGASLC35D1ALG14FUT8PIGNAbout this report →
- Syndromic CraniosynostosisReads 6 of these genesFGFR3ERFFGFR2TWIST1SMOWDR35About this report →
- Intellectual DisabilityReads 18 of these genesKDM6BPRMT7THOC2RPL10ASXL3CDK13About this report →
- Hereditary Arterial CalcificationReads 2 of these genesABCC6ENPP1About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 2 of these genesPHOX2BRETAbout this report →
- Monogenic Precocious PubertyReads 2 of these genesDLK1MKRN3About this report →
- Congenital Cranial Dysinnervation DisordersReads 3 of these genesKIF21ATUBA1AMAFBAbout this report →
- Congenital Diarrhoeas & EnteropathiesReads 4 of these genesSLC9A3SPINT2PLVAPSLC26A3About this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- Alveolar Capillary Dysplasia with Misalignment of Pulmonary VeinsReads 1 of these genesFOXF1About this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- Congenital Central Hypoventilation SyndromeReads 1 of these genesPHOX2BAbout this report →
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- Hereditary HypospadiasReads 1 of these genesMAMLD1About this report →
- Hereditary Leiomyomatosis and Renal Cell CancerReads 1 of these genesFHAbout this report →
- HypophosphatasiaReads 1 of these genesALPLAbout this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Epilepsy (Full Panel)Reads 13 of these genesATP1A2PIGQSLC2A1STRADATHOC2PIGAAbout this report →
- Epidermolysis BullosaReads 4 of these genesPLECDSTITGA6ITGB4About this report →
- GPI Anchor Biosynthesis DefectsReads 4 of these genesPIGQPIGAPIGNPIGYAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 2 of these genesHBA1HBA2About this report →
- ThalassaemiaReads 2 of these genesHBA1HBA2About this report →
- Ehlers-Danlos SyndromeReads 4 of these genesB3GALT6FKBP14COL1A1COL1A2About this report →
- LipodystrophyReads 3 of these genesAKT2LMNAZMPSTE24About this report →
- Dilated CardiomyopathyReads 6 of these genesNEXNRAF1LMNAPPP1R13LMYPNSYNE1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 5 of these genesACTBSCN4ASLC2A1TOR1AVAC14About this report →
- Aortic AneurysmReads 3 of these genesFBN1MYH11MYLKAbout this report →
- Hereditary Orofacial CleftingReads 2 of these genesIRF6MSX1About this report →
- Waardenburg SyndromeReads 2 of these genesEDN3EDNRBAbout this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 3 of these genesADAMTS3MDFICPIEZO1About this report →
- Congenital Muscular DystrophiesReads 4 of these genesDOK7DPM2ITGA7SELENONAbout this report →
- Disorders of Glycine & Serine MetabolismReads 2 of these genesPHGDHPSAT1About this report →
- PolycythemiaReads 2 of these genesHBA1HBA2About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 1 of these genesNOTCH3About this report →
- Congenital Intestinal Atresia & Short BowelReads 1 of these genesTTC7AAbout this report →
- Hereditary Gingival FibromatosisReads 1 of these genesSOS1About this report →
- Hereditary Multiple OsteochondromasReads 1 of these genesEXT2About this report →
- Lung CancerReads 1 of these genesEGFRAbout this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Myotonic DystrophyReads 1 of these genesDMPKAbout this report →
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 1 of these genesPHOX2BAbout this report →
- Niemann-Pick Disease Type CReads 1 of these genesNPC2About this report →
- Pseudoxanthoma ElasticumReads 1 of these genesABCC6About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL2A1SLC26A2About this report →
- Congenital Diaphragmatic Hernia (Monogenic)Reads 1 of these genesALDH1A2About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7AAbout this report →
- Familial Hemiplegic MigraineReads 1 of these genesATP1A2About this report →
- Familial Periodic ParalysisReads 1 of these genesSCN4AAbout this report →
- Thyroid Hormone Resistance, Transport & Metabolism DefectsReads 1 of these genesSLC16A2About this report →
- Spinal Muscular AtrophyReads 3 of these genesBICD2TSEN54ATP7AAbout this report →
- OsteopetrosisReads 2 of these genesCLCN7AMER1About this report →
- NeurofibromatosisReads 1 of these genesLZTR1About this report →
- Joubert Syndrome And Related DisordersReads 3 of these genesKIF7OFD1KIAA0586About this report →
- Ectodermal DysplasiasReads 2 of these genesNECTIN1TP63About this report →
- Fanconi AnemiaReads 2 of these genesFANCBFANCFAbout this report →
- Charcot-Marie-Tooth DiseaseReads 4 of these genesDNM2ATP7AFIG4LMNAAbout this report →
- PancreatitisReads 1 of these genesTRPV6About this report →
- Autoimmune DiseaseReads 2 of these genesKRASCHRNGAbout this report →
- Hypogonadotropic HypogonadismReads 3 of these genesOTX2CHD7MAGEL2About this report →
- Female InfertilityReads 3 of these genesTRIP13TP63HSD17B4About this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 1 of these genesKCNK3About this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesEGFRAbout this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 1 of these genesHSD17B4About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 3 of these genesWDR81KIAA0586SYNE1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 2 of these genesOTX2SMOAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 1 of these genesWDR35About this report →
- Hypodontia and AnodontiaReads 1 of these genesMSX1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 2 of these genesSOD1FIG4About this report →
- Thyroid CancerReads 2 of these genesTRPV6RETAbout this report →
- GlomerulosclerosisReads 1 of these genesCRB2About this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesENPP1About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesRETAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Red Blood Cell Membrane DisordersReads 1 of these genesPIEZO1About this report →
- Inherited ThrombocytopeniasReads 2 of these genesACTBGP1BBAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesPLECLMNAAbout this report →
- Osteogenesis ImperfectaReads 2 of these genesCOL1A1COL1A2About this report →
- Other Inborn Errors of ImmunityReads 5 of these genesIKZF1KRASRELTBX1SKIC3About this report →
- Autism Spectrum DisorderReads 1 of these genesCHD8About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesMAGEL2About this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BBAbout this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 1 of these genesIKZF1About this report →
- Focal Segmental GlomerulosclerosisReads 1 of these genesCRB2About this report →
- Hereditary Macular DystrophiesReads 1 of these genesPRDM13About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesRETAbout this report →
- Marfan Like SyndromesReads 1 of these genesFBN1About this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 1 of these genesCOASYAbout this report →
- DNA Repair DiseaseReads 2 of these genesFANCBFANCFAbout this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesPPP1R13LAbout this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesSOX17About this report →
- Familial HypomagnesemiaReads 1 of these genesTRPV6About this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesZIC3About this report →
- HyperinsulinismReads 1 of these genesINSRAbout this report →
- Polycystic Kidney DiseaseReads 1 of these genesALG9About this report →
- Severe Congenital NeutropeniaReads 1 of these genesCLPBAbout this report →
- Urinary and Renal System TumourReads 1 of these genesRETAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesRYR1About this report →
- Diamond-Blackfan AnemiaReads 1 of these genesRPL11About this report →
- Lysosomal Storage DiseaseReads 2 of these genesNPC2GBA1About this report →
- Glycogen Storage DiseaseReads 1 of these genesGBE1About this report →
- Parkinson DiseaseReads 1 of these genesGBA1About this report →
- Primary Mitochondrial DiseaseReads 3 of these genesRMND1TFAMSLC25A26About this report →
- Cutis LaxaReads 1 of these genesATP7AAbout this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesKIDINS220ABCD1About this report →
- Congenital HypothyroidismReads 1 of these genesFOXE1About this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesMTHFRAbout this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesNPHP3About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 1 of these genesDSTAbout this report →
- Hearing Loss and DeafnessReads 2 of these genesTBC1D24COL11A2About this report →
- VitreoretinopathyReads 1 of these genesCOL2A1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesOTX2About this report →
- Diabetes MellitusReads 1 of these genesAKT2About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 1 of these genesSKIC3About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesABCD1About this report →
- Retinitis PigmentosaReads 1 of these genesOFD1About this report →
Olvassa el a(z) High levels of amniotic fluid nevű génhez kapcsolódó információkat, valamint a genomja többi részét egyetlen teszttel.
449 $-tólIngyenes szállítás · Eredmények 6–8 hét alatt
Kérem a Genome Testemet335 gén kapcsolódik ehhez: High levels of amniotic fluid
Ezeknek a géneknek a változásai olyan ritka betegségeket okoznak, amelyekben előfordul a(z) High levels of amniotic fluid. A tulajdonsággal rendelkező emberek többségének nincs ezek közül egyik betegsége sem, a listán szereplő gének pedig semmit nem mondanak el senki saját genomjáról.
| Gén | Milyen gyakran fordul elő | Betegségek |
|---|---|---|
| ACTBactin beta | Mindig | 1 betegségben |
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Mindig | 1 betegségben |
| AMMECR1AMMECR nuclear protein 1 | Mindig | 1 betegségben |
| ANO1anoctamin 1 | Mindig | 1 betegségben |
| ARID2AT-rich interaction domain 2 | Mindig | 1 betegségben |
| ASCC1activating signal cointegrator 1 complex subunit 1 | Mindig | 1 betegségben |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | Mindig | 1 betegségben |
| B3GALT6beta-1,3-galactosyltransferase 6 | Mindig | 1 betegségben |
| CALCRLcalcitonin receptor like receptor | Mindig | 1 betegségben |
| CHASERRCHD2 adjacent suppressive regulatory RNA | Mindig | 1 betegségben |
| CRNKL1crooked neck pre-mRNA splicing factor 1 | Mindig | 1 betegségben |
| DMRT2doublesex and mab-3 related transcription factor 2 | Mindig | 1 betegségben |
| DNM2dynamin 2 | Mindig | 2 betegségben |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Mindig | 1 betegségben |
| EGFRepidermal growth factor receptor | Mindig | 1 betegségben |
| EXTL3exostosin like glycosyltransferase 3 | Mindig | 2 betegségben |
| FGFR3fibroblast growth factor receptor 3 | Mindig | 5 betegségben |
| FHfumarate hydratase | Mindig | 2 betegségben |
| FKBP14FKBP prolyl isomerase 14 | Mindig | 1 betegségben |
| GBE11,4-alpha-glucan branching enzyme 1 | Mindig | 1 betegségben |
| GLDNgliomedin | Mindig | 2 betegségben |
| GPC3glypican 3 | Mindig | 2 betegségben |
| IBA57iron-sulfur cluster assembly factor IBA57 | Mindig | 2 betegségben |
| IKZF1IKAROS family zinc finger 1 | Mindig | 1 betegségben |
| INSRinsulin receptor | Mindig | 1 betegségben |
| JKAMPJNK1/MAPK8 associated membrane protein | Mindig | 1 betegségben |
| KDM6Blysine demethylase 6B | Mindig | 1 betegségben |
| LMOD1leiomodin 1 | Mindig | 2 betegségben |
| MED16mediator complex subunit 16 | Mindig | 1 betegségben |
| MYOD1myogenic differentiation 1 | Mindig | 2 betegségben |
| NEXNnexilin F-actin binding protein | Mindig | 1 betegségben |
| NOTCH3notch receptor 3 | Mindig | 1 betegségben |
| PAICSphosphoribosylaminoimidazole carboxylase and phosphoribosylaminoimidazolesuccinocarboxamide synthase | Mindig | 1 betegségben |
| PIGQphosphatidylinositol glycan anchor biosynthesis class Q | Mindig | 1 betegségben |
| PLAAphospholipase A2 activating protein | Mindig | 1 betegségben |
| PPP1CBprotein phosphatase 1 catalytic subunit beta | Mindig | 1 betegségben |
| PRMT7protein arginine methyltransferase 7 | Mindig | 1 betegségben |
| PRRX1paired related homeobox 1 | Mindig | 2 betegségben |
| REREarginine-glutamic acid dipeptide repeats | Mindig | 1 betegségben |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Mindig | 3 betegségben |
További 295 gén megjelenítése
| Gén | Milyen gyakran fordul elő | Betegségek |
|---|---|---|
| SCYL2SCY1 like pseudokinase 2 | Mindig | 1 betegségben |
| SLC12A1solute carrier family 12 member 1 | Mindig | 1 betegségben |
| SLC27A4solute carrier family 27 member 4 | Mindig | 1 betegségben |
| SLC2A1solute carrier family 2 member 1 | Mindig | 1 betegségben |
| SLC9A3solute carrier family 9 member A3 | Mindig | 1 betegségben |
| SOD1superoxide dismutase 1 | Mindig | 1 betegségben |
| SOS1SOS Ras/Rac guanine nucleotide exchange factor 1 | Mindig | 1 betegségben |
| STRADASTE20 related adaptor alpha | Mindig | 2 betegségben |
| TBC1D32TBC1 domain family member 32 | Mindig | 1 betegségben |
| THOC2THO complex subunit 2 | Mindig | 1 betegségben |
| TM2D3TM2 domain containing 3 | Mindig | 1 betegségben |
| TOR1Atorsin family 1 member A | Mindig | 1 betegségben |
| ZBTB42zinc finger and BTB domain containing 42 | Mindig | 1 betegségben |
| ZIC3Zic family zinc finger 3 | Mindig | 2 betegségben |
| BUB1BUB1 mitotic checkpoint serine/threonine kinase | Nagyon gyakran (80–99%) | 1 betegségben |
| BUB1BBUB1 mitotic checkpoint serine/threonine kinase B | Nagyon gyakran (80–99%) | 1 betegségben |
| BUB3BUB3 mitotic checkpoint protein | Nagyon gyakran (80–99%) | 1 betegségben |
| CEP57centrosomal protein 57 | Nagyon gyakran (80–99%) | 1 betegségben |
| DLK1delta like non-canonical Notch ligand 1 | Nagyon gyakran (80–99%) | 3 betegségben |
| FANCBFA complementation group B | Nagyon gyakran (80–99%) | 1 betegségben |
| FOXE1forkhead box E1 | Nagyon gyakran (80–99%) | 2 betegségben |
| HOXD13homeobox D13 | Nagyon gyakran (80–99%) | 1 betegségben |
| HYLS1HYLS1 centriolar and ciliogenesis associated | Nagyon gyakran (80–99%) | 2 betegségben |
| INPPL1inositol polyphosphate phosphatase like 1 | Nagyon gyakran (80–99%) | 2 betegségben |
| KIF7kinesin family member 7 | Nagyon gyakran (80–99%) | 1 betegségben |
| MEG3maternally expressed 3 | Nagyon gyakran (80–99%) | 3 betegségben |
| MUSKmuscle associated receptor tyrosine kinase | Nagyon gyakran (80–99%) | 2 betegségben |
| ODC1ornithine decarboxylase 1 | Nagyon gyakran (80–99%) | 2 betegségben |
| OTX2orthodenticle homeobox 2 | Nagyon gyakran (80–99%) | 1 betegségben |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Nagyon gyakran (80–99%) | 1 betegségben |
| PLECplectin | Nagyon gyakran (80–99%) | 3 betegségben |
| PTH1Rparathyroid hormone 1 receptor | Nagyon gyakran (80–99%) | 2 betegségben |
| RSPO2R-spondin 2 | Nagyon gyakran (80–99%) | 1 betegségben |
| RTL1retrotransposon Gag like 1 | Nagyon gyakran (80–99%) | 3 betegségben |
| SLC35D1solute carrier family 35 member D1 | Nagyon gyakran (80–99%) | 2 betegségben |
| TBX4T-box transcription factor 4 | Nagyon gyakran (80–99%) | 1 betegségben |
| TRIP13thyroid hormone receptor interactor 13 | Nagyon gyakran (80–99%) | 1 betegségben |
| WNT3Wnt family member 3 | Nagyon gyakran (80–99%) | 1 betegségben |
| ABCC6ATP binding cassette subfamily C member 6 | Gyakran (30–79%) | 1 betegségben |
| ACTA1actin alpha 1, skeletal muscle | Gyakran (30–79%) | 6 betegségben |
| ACTG2actin gamma 2, smooth muscle | Gyakran (30–79%) | 2 betegségben |
| ADAMTSL2ADAMTS like 2 | Gyakran (30–79%) | 1 betegségben |
| ADGRG6adhesion G protein-coupled receptor G6 | Gyakran (30–79%) | 1 betegségben |
| AKT2AKT serine/threonine kinase 2 | Gyakran (30–79%) | 1 betegségben |
| ALDH1A2aldehyde dehydrogenase 1 family member A2 | Gyakran (30–79%) | 1 betegségben |
| ALG14ALG14 UDP-N-acetylglucosaminyltransferase subunit | Gyakran (30–79%) | 1 betegségben |
| ATAD3AATPase family AAA domain containing 3A | Gyakran (30–79%) | 1 betegségben |
| ATP6V0A1ATPase H+ transporting V0 subunit a1 | Gyakran (30–79%) | 1 betegségben |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Gyakran (30–79%) | 1 betegségben |
| BICD2BICD cargo adaptor 2 | Gyakran (30–79%) | 1 betegségben |
| BIN1bridging integrator 1 | Gyakran (30–79%) | 1 betegségben |
| BSNDbarttin CLCNK type accessory subunit beta | Gyakran (30–79%) | 2 betegségben |
| CHD7chromodomain helicase DNA binding protein 7 | Gyakran (30–79%) | 2 betegségben |
| CLCN7Cl-/H+ antiporter 7 | Gyakran (30–79%) | 1 betegségben |
| CLCNKAchloride voltage-gated channel Ka | Gyakran (30–79%) | 2 betegségben |
| CLCNKBchloride voltage-gated channel Kb | Gyakran (30–79%) | 2 betegségben |
| CNTNAP1contactin associated protein 1 | Gyakran (30–79%) | 2 betegségben |
| COL2A1collagen type II alpha 1 chain | Gyakran (30–79%) | 4 betegségben |
| DHCR77-dehydrocholesterol reductase | Gyakran (30–79%) | 1 betegségben |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Gyakran (30–79%) | 1 betegségben |
| DOK7docking protein 7 | Gyakran (30–79%) | 1 betegségben |
| DSTdystonin | Gyakran (30–79%) | 2 betegségben |
| DTYMKdeoxythymidylate kinase | Gyakran (30–79%) | 1 betegségben |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Gyakran (30–79%) | 1 betegségben |
| ERFETS2 repressor factor | Gyakran (30–79%) | 1 betegségben |
| FANCFFA complementation group F | Gyakran (30–79%) | 1 betegségben |
| FBN1fibrillin 1 | Gyakran (30–79%) | 1 betegségben |
| FGFR2fibroblast growth factor receptor 2 | Gyakran (30–79%) | 1 betegségben |
| FLNBfilamin B | Gyakran (30–79%) | 4 betegségben |
| FUT8fucosyltransferase 8 | Gyakran (30–79%) | 1 betegségben |
| GLE1GLE1 RNA export mediator | Gyakran (30–79%) | 1 betegségben |
| GPC4glypican 4 | Gyakran (30–79%) | 1 betegségben |
| GRM7glutamate metabotropic receptor 7 | Gyakran (30–79%) | 1 betegségben |
| HBA1hemoglobin subunit alpha 1 | Gyakran (30–79%) | 1 betegségben |
| HBA2hemoglobin subunit alpha 2 | Gyakran (30–79%) | 1 betegségben |
| HIC1HIC ZBTB transcriptional repressor 1 | Gyakran (30–79%) | 1 betegségben |
| HRASHRas proto-oncogene, GTPase | Gyakran (30–79%) | 2 betegségben |
| IFT56intraflagellar transport 56 | Gyakran (30–79%) | 1 betegségben |
| ITGA6integrin subunit alpha 6 | Gyakran (30–79%) | 2 betegségben |
| ITGB4integrin subunit beta 4 | Gyakran (30–79%) | 3 betegségben |
| KAT6Blysine acetyltransferase 6B | Gyakran (30–79%) | 2 betegségben |
| KCNJ6potassium inwardly rectifying channel subfamily J member 6 | Gyakran (30–79%) | 2 betegségben |
| KCNK3potassium two pore domain channel subfamily K member 3 | Gyakran (30–79%) | 1 betegségben |
| KDM6Alysine demethylase 6A | Gyakran (30–79%) | 1 betegségben |
| KIDINS220kinase D interacting substrate 220 | Gyakran (30–79%) | 2 betegségben |
| KIF21Akinesin family member 21A | Gyakran (30–79%) | 1 betegségben |
| KLHL40kelch like family member 40 | Gyakran (30–79%) | 2 betegségben |
| KLHL41kelch like family member 41 | Gyakran (30–79%) | 5 betegségben |
| KMT2Dlysine methyltransferase 2D | Gyakran (30–79%) | 2 betegségben |
| KRASKRas proto-oncogene, GTPase | Gyakran (30–79%) | 3 betegségben |
| LBRlamin B receptor | Gyakran (30–79%) | 1 betegségben |
| LMOD3leiomodin 3 | Gyakran (30–79%) | 3 betegségben |
| LTBP3latent transforming growth factor beta binding protein 3 | Gyakran (30–79%) | 2 betegségben |
| LZTR1leucine zipper like post translational regulator 1 | Gyakran (30–79%) | 1 betegségben |
| MAGEL2MAGE family member L2 | Gyakran (30–79%) | 2 betegségben |
| MAMLD1mastermind like domain containing 1 | Gyakran (30–79%) | 1 betegségben |
| MAP2K2mitogen-activated protein kinase kinase 2 | Gyakran (30–79%) | 2 betegségben |
| MDFICMyoD family inhibitor domain containing | Gyakran (30–79%) | 1 betegségben |
| MTHFRmethylenetetrahydrofolate reductase | Gyakran (30–79%) | 1 betegségben |
| MTM1myotubularin 1 | Gyakran (30–79%) | 3 betegségben |
| MTMR14myotubularin related protein 14 | Gyakran (30–79%) | 1 betegségben |
| MYF6myogenic factor 6 | Gyakran (30–79%) | 1 betegségben |
| MYH11myosin heavy chain 11 | Gyakran (30–79%) | 1 betegségben |
| MYL1myosin light chain 1 | Gyakran (30–79%) | 1 betegségben |
| MYLKmyosin light chain kinase | Gyakran (30–79%) | 1 betegségben |
| NEBnebulin | Gyakran (30–79%) | 6 betegségben |
| NPHP3nephrocystin 3 | Gyakran (30–79%) | 1 betegségben |
| NRASNRAS proto-oncogene, GTPase | Gyakran (30–79%) | 1 betegségben |
| NUP88nucleoporin 88 | Gyakran (30–79%) | 2 betegségben |
| OTUD5OTU deubiquitinase 5 | Gyakran (30–79%) | 1 betegségben |
| PAFAH1B1platelet activating factor acetylhydrolase 1b regulatory subunit 1 | Gyakran (30–79%) | 2 betegségben |
| PCGF2polycomb group ring finger 2 | Gyakran (30–79%) | 1 betegségben |
| PHACTR1phosphatase and actin regulator 1 | Gyakran (30–79%) | 1 betegségben |
| PHGDHphosphoglycerate dehydrogenase | Gyakran (30–79%) | 1 betegségben |
| PI4KAphosphatidylinositol 4-kinase alpha | Gyakran (30–79%) | 1 betegségben |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Gyakran (30–79%) | 2 betegségben |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Gyakran (30–79%) | 1 betegségben |
| PRDM13PR/SET domain 13 | Gyakran (30–79%) | 1 betegségben |
| PSAT1phosphoserine aminotransferase 1 | Gyakran (30–79%) | 1 betegségben |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Gyakran (30–79%) | 1 betegségben |
| RAPSNreceptor associated protein of the synapse | Gyakran (30–79%) | 1 betegségben |
| RIT1Ras like without CAAX 1 | Gyakran (30–79%) | 1 betegségben |
| RMND1required for meiotic nuclear division 1 homolog | Gyakran (30–79%) | 1 betegségben |
| RPL10ribosomal protein L10 | Gyakran (30–79%) | 2 betegségben |
| RRAS2RAS related 2 | Gyakran (30–79%) | 1 betegségben |
| RYR1ryanodine receptor 1 | Gyakran (30–79%) | 3 betegségben |
| SCN8Asodium voltage-gated channel alpha subunit 8 | Gyakran (30–79%) | 1 betegségben |
| SEMA3Esemaphorin 3E | Gyakran (30–79%) | 1 betegségben |
| SLC18A3solute carrier family 18 member A3 | Gyakran (30–79%) | 1 betegségben |
| SLC25A12solute carrier family 25 member 12 | Gyakran (30–79%) | 1 betegségben |
| SLC25A46solute carrier family 25 member 46 | Gyakran (30–79%) | 1 betegségben |
| SLC26A2solute carrier family 26 member 2 | Gyakran (30–79%) | 3 betegségben |
| SOX9SRY-box transcription factor 9 | Gyakran (30–79%) | 2 betegségben |
| SPINT2serine peptidase inhibitor, Kunitz type 2 | Gyakran (30–79%) | 1 betegségben |
| SPRED2sprouty related EVH1 domain containing 2 | Gyakran (30–79%) | 1 betegségben |
| SZT2SZT2 subunit of KICSTOR complex | Gyakran (30–79%) | 1 betegségben |
| TBC1D24TBC1 domain family member 24 | Gyakran (30–79%) | 1 betegségben |
| TFAMtranscription factor A, mitochondrial | Gyakran (30–79%) | 1 betegségben |
| TMCO1transmembrane and coiled-coil domains 1 | Gyakran (30–79%) | 2 betegségben |
| TNNC2troponin C2, fast skeletal type | Gyakran (30–79%) | 1 betegségben |
| TPM3tropomyosin 3 | Gyakran (30–79%) | 3 betegségben |
| TRIP11thyroid hormone receptor interactor 11 | Gyakran (30–79%) | 2 betegségben |
| TRPV6transient receptor potential cation channel subfamily V member 6 | Gyakran (30–79%) | 1 betegségben |
| TSEN54tRNA splicing endonuclease subunit 54 | Gyakran (30–79%) | 2 betegségben |
| TTC7Atetratricopeptide repeat domain 7A | Gyakran (30–79%) | 2 betegségben |
| TUBA1Atubulin alpha 1a | Gyakran (30–79%) | 1 betegségben |
| TWIST1twist family bHLH transcription factor 1 | Gyakran (30–79%) | 1 betegségben |
| VANGL2VANGL planar cell polarity protein 2 | Gyakran (30–79%) | 1 betegségben |
| YWHAEtyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein epsilon | Gyakran (30–79%) | 1 betegségben |
| ABCD1ATP binding cassette subfamily D member 1 | Néha (5–29%) | 1 betegségben |
| ADARB1adenosine deaminase RNA specific B1 | Néha (5–29%) | 1 betegségben |
| ADAT3adenosine deaminase tRNA specific 3 | Néha (5–29%) | 1 betegségben |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Néha (5–29%) | 1 betegségben |
| ARVCFARVCF delta catenin family member | Néha (5–29%) | 1 betegségben |
| ASCL1achaete-scute family bHLH transcription factor 1 | Néha (5–29%) | 1 betegségben |
| ASXL3ASXL transcriptional regulator 3 | Néha (5–29%) | 1 betegségben |
| ATP7AATPase copper transporting alpha | Néha (5–29%) | 1 betegségben |
| B3GLCTbeta 3-glucosyltransferase | Néha (5–29%) | 2 betegségben |
| BCL11ABCL11 transcription factor A | Néha (5–29%) | 1 betegségben |
| CBLCbl proto-oncogene | Néha (5–29%) | 1 betegségben |
| CCDC47coiled-coil domain containing 47 | Néha (5–29%) | 1 betegségben |
| CD96CD96 molecule | Néha (5–29%) | 1 betegségben |
| CDC42BPBCDC42 binding protein kinase beta | Néha (5–29%) | 1 betegségben |
| CDK13cyclin dependent kinase 13 | Néha (5–29%) | 1 betegségben |
| CFL2cofilin 2 | Néha (5–29%) | 1 betegségben |
| CHD8chromodomain helicase DNA binding protein 8 | Néha (5–29%) | 1 betegségben |
| CILK1ciliogenesis associated kinase 1 | Néha (5–29%) | 1 betegségben |
| CLPBClpB family mitochondrial disaggregase | Néha (5–29%) | 1 betegségben |
| COASYCoenzyme A synthase | Néha (5–29%) | 1 betegségben |
| COL11A2collagen type XI alpha 2 chain | Néha (5–29%) | 1 betegségben |
| COL1A1collagen type I alpha 1 chain | Néha (5–29%) | 1 betegségben |
| COL1A2collagen type I alpha 2 chain | Néha (5–29%) | 1 betegségben |
| COMTcatechol-O-methyltransferase | Néha (5–29%) | 1 betegségben |
| CREBBPCREB binding lysine acetyltransferase | Néha (5–29%) | 2 betegségben |
| CRELD1CRELD disulfide isomerase 1 | Néha (5–29%) | 1 betegségben |
| CSNK2A1casein kinase 2 alpha 1 | Néha (5–29%) | 1 betegségben |
| DMPKDM1 protein kinase | Néha (5–29%) | 2 betegségben |
| DPF2double PHD fingers 2 | Néha (5–29%) | 1 betegségben |
| DPH5diphthamide biosynthesis 5 | Néha (5–29%) | 1 betegségben |
| DPM2dolichyl-phosphate mannosyltransferase subunit 2, regulatory | Néha (5–29%) | 1 betegségben |
| DYNC2I2dynein 2 intermediate chain 2 | Néha (5–29%) | 1 betegségben |
| ECE1endothelin converting enzyme 1 | Néha (5–29%) | 1 betegségben |
| EDN3endothelin 3 | Néha (5–29%) | 1 betegségben |
| EDNRBendothelin receptor type B | Néha (5–29%) | 1 betegségben |
| EP300EP300 lysine acetyltransferase | Néha (5–29%) | 2 betegségben |
| ERBB2erb-b2 receptor tyrosine kinase 2 | Néha (5–29%) | 1 betegségben |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Néha (5–29%) | 2 betegségben |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Néha (5–29%) | 2 betegségben |
| EXT2exostosin glycosyltransferase 2 | Néha (5–29%) | 1 betegségben |
| FIG4FIG4 phosphoinositide 5-phosphatase | Néha (5–29%) | 2 betegségben |
| GDNFglial cell derived neurotrophic factor | Néha (5–29%) | 1 betegségben |
| GP1BBglycoprotein Ib platelet subunit beta | Néha (5–29%) | 1 betegségben |
| HACD13-hydroxyacyl-CoA dehydratase 1 | Néha (5–29%) | 1 betegségben |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Néha (5–29%) | 1 betegségben |
| HIRAhistone cell cycle regulator | Néha (5–29%) | 1 betegségben |
| HSPG2heparan sulfate proteoglycan 2 | Néha (5–29%) | 1 betegségben |
| IPO8importin 8 | Néha (5–29%) | 1 betegségben |
| ITGA7integrin subunit alpha 7 | Néha (5–29%) | 1 betegségben |
| JMJD1Cjumonji domain containing 1C | Néha (5–29%) | 1 betegségben |
| KDM3Blysine demethylase 3B | Néha (5–29%) | 1 betegségben |
| LMNAlamin A/C | Néha (5–29%) | 1 betegségben |
| MADDMAP kinase activating death domain | Néha (5–29%) | 1 betegségben |
| MAFBMAF bZIP transcription factor B | Néha (5–29%) | 1 betegségben |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Néha (5–29%) | 1 betegségben |
| MKRN3makorin ring finger protein 3 | Néha (5–29%) | 1 betegségben |
| MOGSmannosyl-oligosaccharide glucosidase | Néha (5–29%) | 1 betegségben |
| MYH3myosin heavy chain 3 | Néha (5–29%) | 2 betegségben |
| MYL2myosin light chain 2 | Néha (5–29%) | 1 betegségben |
| NALCNsodium leak channel, non-selective | Néha (5–29%) | 1 betegségben |
| NPAP1nuclear pore associated protein 1 | Néha (5–29%) | 1 betegségben |
| NPC2NPC intracellular cholesterol transporter 2 | Néha (5–29%) | 1 betegségben |
| NRCAMneuronal cell adhesion molecule | Néha (5–29%) | 1 betegségben |
| NRTNneurturin | Néha (5–29%) | 1 betegségben |
| OFD1OFD1 centriole and centriolar satellite protein | Néha (5–29%) | 1 betegségben |
| PHOX2Bpaired like homeobox 2B | Néha (5–29%) | 1 betegségben |
| PPP1R13Lprotein phosphatase 1 regulatory subunit 13 like | Néha (5–29%) | 1 betegségben |
| PWAR1Prader Willi/Angelman region RNA 1 | Néha (5–29%) | 1 betegségben |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Néha (5–29%) | 1 betegségben |
| RAB34RAB34, member RAS oncogene family | Néha (5–29%) | 1 betegségben |
| RELREL proto-oncogene, NF-kB subunit | Néha (5–29%) | 1 betegségben |
| RETret proto-oncogene | Néha (5–29%) | 2 betegségben |
| RREB1ras responsive element binding protein 1 | Néha (5–29%) | 1 betegségben |
| SEC24CSEC24 homolog C, COPII component | Néha (5–29%) | 1 betegségben |
| SELENONselenoprotein N | Néha (5–29%) | 1 betegségben |
| SEMA3Csemaphorin 3C | Néha (5–29%) | 1 betegségben |
| SEMA3Dsemaphorin 3D | Néha (5–29%) | 1 betegségben |
| SGSM3small G protein signaling modulator 3 | Néha (5–29%) | 1 betegségben |
| SHOC2SHOC2 leucine rich repeat scaffold protein | Néha (5–29%) | 1 betegségben |
| SMOsmoothened, frizzled class receptor | Néha (5–29%) | 1 betegségben |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Néha (5–29%) | 1 betegségben |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Néha (5–29%) | 1 betegségben |
| SOX17SRY-box transcription factor 17 | Néha (5–29%) | 1 betegségben |
| SPOPspeckle type BTB/POZ protein | Néha (5–29%) | 1 betegségben |
| SREBF1sterol regulatory element binding transcription factor 1 | Néha (5–29%) | 1 betegségben |
| TBCDtubulin folding cofactor D | Néha (5–29%) | 1 betegségben |
| TBCKTBC1 domain containing kinase | Néha (5–29%) | 1 betegségben |
| TBX1T-box transcription factor 1 | Néha (5–29%) | 1 betegségben |
| TPM2tropomyosin 2 | Néha (5–29%) | 3 betegségben |
| TRAPPC12trafficking protein particle complex subunit 12 | Néha (5–29%) | 1 betegségben |
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Néha (5–29%) | 1 betegségben |
| VAC14VAC14 component of PIKFYVE complex | Néha (5–29%) | 1 betegségben |
| WBP4WW domain binding protein 4 | Néha (5–29%) | 1 betegségben |
| WDR81WD repeat domain 81 | Néha (5–29%) | 1 betegségben |
| XPO1exportin 1 | Néha (5–29%) | 1 betegségben |
| ZFXzinc finger protein X-linked | Néha (5–29%) | 1 betegségben |
| ZMPSTE24zinc metallopeptidase STE24 | Néha (5–29%) | 2 betegségben |
| ZNF699zinc finger protein 699 | Néha (5–29%) | 1 betegségben |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Ritkán (1–4%) | 2 betegségben |
| AQP2aquaporin 2 | Ritkán (1–4%) | 1 betegségben |
| AVPR2arginine vasopressin receptor 2 | Ritkán (1–4%) | 1 betegségben |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Ritkán (1–4%) | 1 betegségben |
| FOXF1forkhead box F1 | Ritkán (1–4%) | 1 betegségben |
| IRF6interferon regulatory factor 6 | Ritkán (1–4%) | 1 betegségben |
| KBTBD13kelch repeat and BTB domain containing 13 | Ritkán (1–4%) | 1 betegségben |
| MSX1msh homeobox 1 | Ritkán (1–4%) | 1 betegségben |
| MYPNmyopalladin | Ritkán (1–4%) | 1 betegségben |
| NECTIN1nectin cell adhesion molecule 1 | Ritkán (1–4%) | 1 betegségben |
| SLC16A2solute carrier family 16 member 2 | Ritkán (1–4%) | 1 betegségben |
| TAF11TATA-box binding protein associated factor 11 | Ritkán (1–4%) | 1 betegségben |
| TP63tumor protein p63 | Ritkán (1–4%) | 1 betegségben |
| ALPLalkaline phosphatase, biomineralization associated | Nincs rögzítve | 1 betegségben |
| AMER1APC membrane recruitment protein 1 | Nincs rögzítve | 1 betegségben |
| ASXL1ASXL transcriptional regulator 1 | Nincs rögzítve | 1 betegségben |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Nincs rögzítve | 1 betegségben |
| CHRNA1cholinergic receptor nicotinic alpha 1 subunit | Nincs rögzítve | 1 betegségben |
| CHRNDcholinergic receptor nicotinic delta subunit | Nincs rögzítve | 1 betegségben |
| CHRNGcholinergic receptor nicotinic gamma subunit | Nincs rögzítve | 1 betegségben |
| CNTN1contactin 1 | Nincs rögzítve | 1 betegségben |
| CRB2crumbs cell polarity complex component 2 | Nincs rögzítve | 1 betegségben |
| DYNC2I1dynein 2 intermediate chain 1 | Nincs rögzítve | 1 betegségben |
| EBPEBP cholestenol delta-isomerase | Nincs rögzítve | 1 betegségben |
| FLVCR2FLVCR choline and putative heme transporter 2 | Nincs rögzítve | 1 betegségben |
| GBA1glucosylceramidase beta 1 | Nincs rögzítve | 1 betegségben |
| HSD17B4hydroxysteroid 17-beta dehydrogenase 4 | Nincs rögzítve | 1 betegségben |
| KCNJ1potassium inwardly rectifying channel subfamily J member 1 | Nincs rögzítve | 1 betegségben |
| KIAA0586KIAA0586 | Nincs rögzítve | 1 betegségben |
| LONP1lon peptidase 1, mitochondrial | Nincs rögzítve | 1 betegségben |
| MAGED2MAGE family member D2 | Nincs rögzítve | 1 betegségben |
| MAP2K1mitogen-activated protein kinase kinase 1 | Nincs rögzítve | 1 betegségben |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Nincs rögzítve | 1 betegségben |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Nincs rögzítve | 1 betegségben |
| PLVAPplasmalemma vesicle associated protein | Nincs rögzítve | 1 betegségben |
| RHDRh blood group D antigen | Nincs rögzítve | 1 betegségben |
| RPL11ribosomal protein L11 | Nincs rögzítve | 1 betegségben |
| SIN3ASIN3 transcription regulator family member A | Nincs rögzítve | 1 betegségben |
| SKIC3SKI3 subunit of superkiller complex | Nincs rögzítve | 1 betegségben |
| SLC25A26solute carrier family 25 member 26 | Nincs rögzítve | 1 betegségben |
| SLC26A3solute carrier family 26 member 3 | Nincs rögzítve | 1 betegségben |
| SMG9SMG9 nonsense mediated mRNA decay factor | Nincs rögzítve | 1 betegségben |
| SNRPBsmall nuclear ribonucleoprotein polypeptides B and B1 | Nincs rögzítve | 1 betegségben |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Nincs rögzítve | 1 betegségben |
| TAPT1transmembrane anterior posterior transformation 1 | Nincs rögzítve | 1 betegségben |
| TRAIPTRAF interacting protein | Nincs rögzítve | 1 betegségben |
| WDR35WD repeat domain 35 | Nincs rögzítve | 1 betegségben |
| ZC4H2zinc finger C4H2-type containing | Nincs rögzítve | 1 betegségben |
Az, hogy milyen gyakran fordul elő a gén valamelyik állapotával élő emberek körében (a leggyakoribb érték, ahogyan a Human Phenotype Ontology rögzíti). Ezek az oldalak tulajdonságokat és az azok mögött álló kutatásokat ismertetik; nem diagnózist jelentenek. A tünetekkel kapcsolatban orvoshoz vagy genetikai tanácsadóhoz érdemes fordulni.
Tágabb tulajdonságok
Forrás
- Human Phenotype Ontology, 2026-09-01 kiadás: a tulajdonság, a nevei, a definíciója és a hozzá kapcsolt gének. További információ: hpo.jax.org.
- Adatkiadás: 2026.10.17-8666dff2.
From traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 470+ physician-ready reports.
Ingyenes szállítás · Eredmények 6–8 hét alatt
