Tulajdonság
High blood pressure
Klinikai név: Hypertension
The presence of chronic increased pressure in the systemic arterial system.
Összefoglaló
- Más néven
- Arterial hypertension, Systemic hypertension
- Szervrendszer
- Abnormality of the cardiovascular system
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/hypertension.json"
page <- fromJSON(url)
page$trait$nameOlvassa el a(z) High blood pressure nevű génhez kapcsolódó információkat, valamint a genomja többi részét egyetlen teszttel.
449 $-tólIngyenes szállítás · Eredmények 6–8 hét alatt
Kérem a Genome Testemet207 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.
- Bardet-Biedl and Alström SyndromesReads 23 of these genesBBS2CEP290SDCCAG8ALMS1ARL6BBIP1About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 15 of these genesCACNA1DCACNA1HHSD11B2KCNJ5PDE3ASCNN1AAbout this report →
- Aortic AneurysmReads 12 of these genesACTA2FBN1FOXE3LOXMFAP5MYH11About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 14 of these genesCEP164IFT54INVSIQCB1NEK8NPHP1About this report →
Show 203 more reports
- Polycystic Kidney DiseaseReads 10 of these genesIFT140DZIP1LNEK8PKHD1ALG5ALG9About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 9 of these genesMAXRETSDHASDHAF2SDHBSDHCAbout this report →
- Basal Ganglia CalcificationReads 7 of these genesJAM2MYORGNAA60PDGFBPDGFRBSLC20A2About this report →
- Malignant Endocrine NeoplasmReads 7 of these genesRETSDHASDHAF2SDHBTP53CDKN1BAbout this report →
- Loeys-Dietz SyndromeReads 6 of these genesSMAD2SMAD3TGFB2TGFB3TGFBR1TGFBR2About this report →
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 7 of these genesC3CD46CFBCFIDGKETHBDAbout this report →
- LipodystrophyReads 8 of these genesPLIN1PPARGLMNACAV1LIPEPLAAT3About this report →
- Marfan Like SyndromesReads 7 of these genesFBN1SMAD2SMAD3TGFB2TGFB3TGFBR1About this report →
- Urinary and Renal System TumourReads 7 of these genesRETSDHASDHAF2SDHBTP53VHLAbout this report →
- Familial HypercholesterolemiaReads 4 of these genesAPOBLDLRLDLRAP1PCSK9About this report →
- Alport SyndromeReads 3 of these genesCOL4A5COL4A3COL4A4About this report →
- HyperlipidemiaReads 6 of these genesABCG5ABCG8APOBLDLRLDLRAP1PCSK9About this report →
- Focal Segmental GlomerulosclerosisReads 5 of these genesACTN4PAX2CD2APINF2TRPC6About this report →
- Rare Hereditary Peripheral NeuropathiesReads 24 of these genesAPOA1FDXRHSPB8LYZWNK1LMNAAbout this report →
- Congenital Adrenal HyperplasiaReads 4 of these genesCYP11B1CYP17A1PORCYP21A2About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 3 of these genesPRKAR1AARMC5PDE11AAbout this report →
- Hereditary Hemorrhagic TelangiectasiaReads 3 of these genesENGSMAD4ACVRL1About this report →
- GlomerulosclerosisReads 4 of these genesACTN4PAX2INF2TRPC6About this report →
- PolycythemiaReads 4 of these genesEPAS1VHLEPORHBBAbout this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 2 of these genesHTRA1NOTCH3About this report →
- Familial Isolated Pituitary Adenoma (FIPA / X-LAG)Reads 2 of these genesAIPGPR101About this report →
- Hereditary Wilms TumourReads 2 of these genesWT1RESTAbout this report →
- Neuroblastoma Predisposition (ALK and PHOX2B)Reads 2 of these genesALKPHOX2BAbout this report →
- Tuberous SclerosisReads 2 of these genesTSC1TSC2About this report →
- Other Inborn Errors of ImmunityReads 20 of these genesSMARCAL1WASC3C4AC4BCD46About this report →
- Kidney CancerReads 4 of these genesSDHBTP53VHLTRIM28About this report →
- Inherited Neurodegenerative DisordersReads 23 of these genesCC2D2ACLCN2HSPB8SLC30A9CEP290MKS1About this report →
- Hereditary AmyloidosisReads 4 of these genesAPOA1APOA4LYZFGAAbout this report →
- Hereditary Arterial CalcificationReads 2 of these genesABCC6ENPP1About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 2 of these genesRETPHOX2BAbout this report →
- Immuno-Osseous DysplasiasReads 2 of these genesSMARCAL1RNU4ATACAbout this report →
- Joubert Syndrome And Related DisordersReads 7 of these genesCC2D2ACEP290NPHP1MKS1TMEM237TMEM67About this report →
- Leigh SyndromeReads 9 of these genesMTFMTNDUFAF6SDHALRPPRCMT-TKMT-ND1About this report →
- Aicardi-Goutieres SyndromeReads 3 of these genesRNU7-1TREX1IFIH1About this report →
- Hepatic Porphyria DisordersReads 3 of these genesHMBSPPOXCPOXAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 6 of these genesADA2RNU7-1TNFAIP3TREX1ACP5IFIH1About this report →
- Cutis LaxaReads 4 of these genesEFEMP2ELNEMILIN1SLC2A10About this report →
- PorphyriaReads 3 of these genesHMBSPPOXCPOXAbout this report →
- Familial Paget Disease of BoneReads 2 of these genesTNFRSF11ATNFRSF11BAbout this report →
- Hereditary Gastrointestinal Stromal TumourReads 2 of these genesSDHBSDHCAbout this report →
- Moyamoya DiseaseReads 2 of these genesGUCY1A1ACTA2About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 2 of these genesDNMT3ANFIXAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 2 of these genesPRKAR1AGNASAbout this report →
- AlkaptonuriaReads 1 of these genesHGDAbout this report →
- Au-Kline SyndromeReads 1 of these genesHNRNPKAbout this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- CEP164-Related CiliopathyReads 1 of these genesCEP164About this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Congenital Central Hypoventilation SyndromeReads 1 of these genesPHOX2BAbout this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- Deficiency of Adenosine Deaminase 2 (DADA2)Reads 1 of these genesADA2About this report →
- Fabry DiseaseReads 1 of these genesGLAAbout this report →
- FDXR-Related Mitochondrial DisorderReads 1 of these genesFDXRAbout this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- Ferguson-Smith Disease (Multiple Self-Healing Squamous Epithelioma)Reads 1 of these genesTGFBR1About this report →
- Fragile X SyndromeReads 1 of these genesFMR1About this report →
- Frontonasal Dysplasia with Alopecia and Genital Anomaly (ALX4)Reads 1 of these genesALX4About this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- Genetic Prion Disease (incl. Fatal Familial Insomnia)Reads 1 of these genesPRNPAbout this report →
- GTP Cyclohydrolase 1 DeficiencyReads 1 of these genesGCH1About this report →
- Hajdu-Cheney SyndromeReads 1 of these genesNOTCH2About this report →
- Hereditary Leiomyomatosis and Renal Cell CancerReads 1 of these genesFHAbout this report →
- Hereditary Thrombocythaemia (JAK2)Reads 1 of these genesJAK2About this report →
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
- Intracranial Berry AneurysmReads 1 of these genesTHSD1About this report →
- KDM1A-Related Neurodevelopmental DisorderReads 1 of these genesKDM1AAbout this report →
- Keutel SyndromeReads 1 of these genesMGPAbout this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- Low phospholipid-associated cholelithiasisReads 1 of these genesABCB4About this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- Nail-Patella SyndromeReads 1 of these genesLMX1BAbout this report →
- NEK8-Related Renal-Hepatic-Pancreatic DysplasiaReads 1 of these genesNEK8About this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- PBX1-Related Kidney and Urinary Tract AnomaliesReads 1 of these genesPBX1About this report →
- Perlman SyndromeReads 1 of these genesDIS3L2About this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- RNU4ATAC Spectrum DisorderReads 1 of these genesRNU4ATACAbout this report →
- Scalp-Ear-Nipple SyndromeReads 1 of these genesKCTD1About this report →
- SH2B3-Related Immune DysregulationReads 1 of these genesSH2B3About this report →
- Short-Rib Thoracic Dysplasia 7 (WDR35)Reads 1 of these genesWDR35About this report →
- Sickle Cell DiseaseReads 1 of these genesHBBAbout this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- SMAD6-Related DisorderReads 1 of these genesSMAD6About this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- TrimethylaminuriaReads 1 of these genesFMO3About this report →
- Von Hippel-Lindau DiseaseReads 1 of these genesVHLAbout this report →
- Werner SyndromeReads 1 of these genesWRNAbout this report →
- Inherited Complement and Properdin DeficienciesReads 4 of these genesC3C4AC4BCFIAbout this report →
- Retinitis PigmentosaReads 8 of these genesBBS2CC2D2AIFT140ARL6CFAP418IFT172About this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 2 of these genesUMODMUC1About this report →
- Bartter DiseaseReads 2 of these genesBSNDCLCNKBAbout this report →
- Type I InterferonopathiesReads 3 of these genesTREX1ACP5IFIH1About this report →
- Syndromic CraniosynostosisReads 4 of these genesFGFR2WDR19PORWDR35About this report →
- Hereditary Optic NeuropathyReads 3 of these genesMT-ND1MT-ND5MT-ND6About this report →
- Inherited Congenital Heart DefectsReads 3 of these genesELNNKX2-5NOTCH1About this report →
- Adams-Oliver SyndromeReads 2 of these genesNOTCH1ARHGAP31About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 2 of these genesMYH11MYLKAbout this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 2 of these genesCAV1BMPR2About this report →
- Inflammatory Bowel Diseases (IBD)Reads 2 of these genesEGFRIL10About this report →
- Charcot-Marie-Tooth DiseaseReads 7 of these genesHSPB8LMNABSCL2EMILIN1FIG4COQ7About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 2 of these genesWDR19WDR35About this report →
- Hereditary HypolipoproteinemiasReads 2 of these genesAPOA1APOBAbout this report →
- Hypodontia and AnodontiaReads 2 of these genesEDALRP6About this report →
- IPEX Syndrome and Other TregopathiesReads 2 of these genesCTLA4DEF6About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 2 of these genesCEP19MC4RAbout this report →
- Thyroid CancerReads 4 of these genesGNASNKX2-5RETMEN1About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 2 of these genesCACNA1DLMNAAbout this report →
- Age-Related Macular DegenerationReads 1 of these genesCFHAbout this report →
- Alagille SyndromeReads 1 of these genesNOTCH2About this report →
- Enlarged Parietal Foramina (MSX2)Reads 1 of these genesALX4About this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 1 of these genesBRCA2About this report →
- Hereditary FibromatosesReads 1 of these genesPDGFRBAbout this report →
- Hereditary Gingival FibromatosisReads 1 of these genesRESTAbout this report →
- Hereditary Multiple OsteochondromasReads 1 of these genesEXT2About this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- Lung CancerReads 1 of these genesEGFRAbout this report →
- Pseudoxanthoma ElasticumReads 1 of these genesABCC6About this report →
- Wiskott-Aldrich Syndrome SpectrumReads 1 of these genesWASAbout this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesFN1XYLT1About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 5 of these genesCC2D2ACEP290MKS1TMEM237TMEM67About this report →
- Autoimmune DiseaseReads 3 of these genesCTLA4TREX1NOD2About this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 3 of these genesWNK1DSTELP1About this report →
- Familial Intrahepatic CholestasisReads 2 of these genesPSKH1ABCB4About this report →
- Meckel SyndromeReads 2 of these genesMKS1TMEM67About this report →
- DNA Repair DiseaseReads 4 of these genesERCC4ERCC6ERCC8BRCA2About this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 2 of these genesPAX2ITGA8About this report →
- Intellectual DisabilityReads 9 of these genesKDM6BATRXCTNNB1MECP2SCAPERSLC16A2About this report →
- Urea Cycle DisorderReads 2 of these genesASLSLC7A7About this report →
- Congenital AfibrinogenemiaReads 1 of these genesFGAAbout this report →
- MedulloblastomaReads 1 of these genesELP1About this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Thyroid Hormone Resistance, Transport & Metabolism DefectsReads 1 of these genesSLC16A2About this report →
- Spinal Muscular AtrophyReads 3 of these genesHSPB8BSCL2EMILIN1About this report →
- Nephrotic SyndromeReads 3 of these genesACTN4LAMB2DGKEAbout this report →
- Lysosomal Storage DiseaseReads 4 of these genesCTSAIDUAGLAGBA1About this report →
- Glycogen Storage DiseaseReads 2 of these genesSLC37A4G6PC1About this report →
- Osteogenesis ImperfectaReads 3 of these genesIFIH1MBTPS2XYLT2About this report →
- Primary Mitochondrial DiseaseReads 6 of these genesDNAJC30MTFMTNDUFAF6LRPPRCCOQ7TMEM70About this report →
- Congenital Disorders of GlycosylationReads 5 of these genesALG9SLC35A2EXT2PIGASLC37A4About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 3 of these genesGCH1NR4A2VAC14About this report →
- MelanomaReads 1 of these genesCDKN2AAbout this report →
- NeurofibromatosisReads 1 of these genesNF1About this report →
- Fanconi AnemiaReads 2 of these genesERCC4BRCA2About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 2 of these genesATRXWT1About this report →
- Other Inherited LeukodystrophiesReads 4 of these genesCLCN2RNU7-1TREX1IFIH1About this report →
- Homocystinuria & Cobalamin DisordersReads 2 of these genesCBSMTRRAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 1 of these genesHBBAbout this report →
- Mosaic Variegated Aneuploidy SyndromeReads 1 of these genesTRIP13About this report →
- ThalassaemiaReads 1 of these genesHBBAbout this report →
- Epilepsy (Full Panel)Reads 6 of these genesDEPDC5MDH2MECP2SLC35A2PIGAHACE1About this report →
- Female InfertilityReads 3 of these genesFMR1TRIP13LARS2About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesNKX2-5About this report →
- Systemic Lupus ErythematosusReads 1 of these genesTREX1About this report →
- VitreoretinopathyReads 2 of these genesCTNNB1XYLT2About this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 1 of these genesCTSAAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesCTLA4About this report →
- Classic Organic AciduriasReads 1 of these genesACAT1About this report →
- Congenital Cranial Dysinnervation DisordersReads 1 of these genesMAFBAbout this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesTERTAbout this report →
- Diabetes MellitusReads 2 of these genesBSCL2MT-TL1About this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR3C1About this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesENPP1About this report →
- Purine & Pyrimidine Metabolism DisordersReads 1 of these genesAPRTAbout this report →
- Limb-Girdle Muscular DystrophyReads 2 of these genesLMNATRIM32About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesFOXE3About this report →
- Familial Pulmonary FibrosisReads 1 of these genesTERTAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesH19About this report →
- ThrombophiliaReads 1 of these genesTHBDAbout this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 1 of these genesCR2About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 1 of these genesIL12BAbout this report →
- Hearing Loss and DeafnessReads 3 of these genesCDH23USP48POU3F4About this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 1 of these genesGCH1About this report →
- Familial HypomagnesemiaReads 1 of these genesCLDN16About this report →
- Usher SyndromeReads 1 of these genesCDH23About this report →
- Severe Congenital NeutropeniaReads 1 of these genesWASAbout this report →
- Dilated CardiomyopathyReads 2 of these genesNRAPLMNAAbout this report →
- Myofibrillar MyopathiesReads 1 of these genesHSPB8About this report →
- OsteopetrosisReads 1 of these genesTNFRSF11AAbout this report →
- Parkinson DiseaseReads 1 of these genesGBA1About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesBRAFH19About this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 1 of these genesHRAbout this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesTHSD1About this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesBSCL2HACE1About this report →
- Ectodermal DysplasiasReads 1 of these genesEDAAbout this report →
- Epidermolysis BullosaReads 1 of these genesDSTAbout this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-5About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGAAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesBSCL2About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesCOL3A1About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 1 of these genesCEP290About this report →
- Noonan SyndromeReads 1 of these genesBRAFAbout this report →
- Dyskeratosis CongenitaReads 1 of these genesTERTAbout this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesLAMB1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesZFXAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesFIG4About this report →
- Inherited ThrombocytopeniasReads 1 of these genesWASAbout this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesMBTPS2About this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
Olvassa el a(z) High blood pressure nevű génhez kapcsolódó információkat, valamint a genomja többi részét egyetlen teszttel.
449 $-tólIngyenes szállítás · Eredmények 6–8 hét alatt
Kérem a Genome Testemet441 gén kapcsolódik ehhez: High blood pressure
Ezeknek a géneknek a változásai olyan ritka betegségeket okoznak, amelyekben előfordul a(z) High blood pressure. 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 |
|---|---|---|
| ACTN4actinin alpha 4 | Mindig | 1 betegségben |
| ADRA2Aadrenoceptor alpha 2A | Mindig | 1 betegségben |
| APOA1apolipoprotein A1 | Mindig | 1 betegségben |
| APOA4apolipoprotein A4 | Mindig | 1 betegségben |
| BBS2Bardet-Biedl syndrome 2 | Mindig | 2 betegségben |
| CACNA1Dcalcium voltage-gated channel subunit alpha1 D | Mindig | 2 betegségben |
| CACNA1Hcalcium voltage-gated channel subunit alpha1 H | Mindig | 1 betegségben |
| CC2D2Acoiled-coil and C2 domain containing 2A | Mindig | 1 betegségben |
| CEP19centrosomal protein 19 | Mindig | 2 betegségben |
| CIDECcell death inducing DFFA like effector c | Mindig | 1 betegségben |
| CIROZciliated left-right organizer protein containing ZP-N domains | Mindig | 1 betegségben |
| CLCN2chloride voltage-gated channel 2 | Mindig | 2 betegségben |
| CORINcorin, serine peptidase | Mindig | 2 betegségben |
| DEPDC5DEP domain containing 5, GATOR1 subcomplex subunit | Mindig | 1 betegségben |
| DHCR77-dehydrocholesterol reductase | Mindig | 1 betegségben |
| DYRK1Bdual specificity tyrosine phosphorylation regulated kinase 1B | Mindig | 1 betegségben |
| ECE1endothelin converting enzyme 1 | Mindig | 1 betegségben |
| EGFRepidermal growth factor receptor | Mindig | 1 betegségben |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Mindig | 2 betegségben |
| FDXRferredoxin reductase | Mindig | 1 betegségben |
| FEM1Bfem-1 homolog B | Mindig | 1 betegségben |
| FGFR2fibroblast growth factor receptor 2 | Mindig | 3 betegségben |
| GUCY1A1guanylate cyclase 1 soluble subunit alpha 1 | Mindig | 2 betegségben |
| HMOX1heme oxygenase 1 | Mindig | 2 betegségben |
| HSD11B2hydroxysteroid 11-beta dehydrogenase 2 | Mindig | 2 betegségben |
| HSPB8heat shock protein family B (small) member 8 | Mindig | 1 betegségben |
| IFT140intraflagellar transport 140 | Mindig | 3 betegségben |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Mindig | 2 betegségben |
| KDM6Blysine demethylase 6B | Mindig | 1 betegségben |
| LAMB2laminin subunit beta 2 | Mindig | 2 betegségben |
| LYZlysozyme | Mindig | 1 betegségben |
| MAFBMAF bZIP transcription factor B | Mindig | 1 betegségben |
| MDM2MDM2 proto-oncogene | Mindig | 1 betegségben |
| NRAPnebulin related anchoring protein | Mindig | 1 betegségben |
| OAS22'-5'-oligoadenylate synthetase 2 | Mindig | 1 betegségben |
| PDE3Aphosphodiesterase 3A | Mindig | 2 betegségben |
| PLD4phospholipase D family member 4 | Mindig | 1 betegségben |
| PLIN1perilipin 1 | Mindig | 2 betegségben |
| PPARGperoxisome proliferator activated receptor gamma | Mindig | 2 betegségben |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Mindig | 4 betegségben |
További 401 gén megjelenítése
| Gén | Milyen gyakran fordul elő | Betegségek |
|---|---|---|
| PSKH1protein serine kinase H1 | Mindig | 1 betegségben |
| PTPMT1protein tyrosine phosphatase mitochondrial 1 | Mindig | 1 betegségben |
| RAB32RAB32, member RAS oncogene family | Mindig | 1 betegségben |
| RDH8retinol dehydrogenase 8 | Mindig | 1 betegségben |
| RFC4replication factor C subunit 4 | Mindig | 1 betegségben |
| RNU5B-1RNA, U5B small nuclear 1 | Mindig | 1 betegségben |
| SCNN1Asodium channel epithelial 1 subunit alpha | Mindig | 2 betegségben |
| SCNN1Bsodium channel epithelial 1 subunit beta | Mindig | 2 betegségben |
| SCNN1Gsodium channel epithelial 1 subunit gamma | Mindig | 2 betegségben |
| SGSM3small G protein signaling modulator 3 | Mindig | 1 betegségben |
| SLC30A9solute carrier family 30 member 9 | Mindig | 1 betegségben |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Mindig | 2 betegségben |
| WASWASP actin nucleation promoting factor | Mindig | 1 betegségben |
| WNK1WNK lysine deficient protein kinase 1 | Mindig | 1 betegségben |
| CEP164centrosomal protein 164 | Nagyon gyakran (80–99%) | 1 betegségben |
| CEP290centrosomal protein 290 | Nagyon gyakran (80–99%) | 2 betegségben |
| CYP11B1cytochrome P450 family 11 subfamily B member 1 | Nagyon gyakran (80–99%) | 4 betegségben |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Nagyon gyakran (80–99%) | 1 betegségben |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Nagyon gyakran (80–99%) | 2 betegségben |
| DZIP1LDAZ interacting zinc finger protein 1 like | Nagyon gyakran (80–99%) | 2 betegségben |
| FLT1fms related receptor tyrosine kinase 1 | Nagyon gyakran (80–99%) | 1 betegségben |
| FN1fibronectin 1 | Nagyon gyakran (80–99%) | 2 betegségben |
| IFT54intraflagellar transport 54 | Nagyon gyakran (80–99%) | 1 betegségben |
| INVSinversin | Nagyon gyakran (80–99%) | 2 betegségben |
| IQCB1IQ motif containing B1 | Nagyon gyakran (80–99%) | 1 betegségben |
| JAK2Janus kinase 2 | Nagyon gyakran (80–99%) | 2 betegségben |
| LMNAlamin A/C | Nagyon gyakran (80–99%) | 5 betegségben |
| LMX1BLIM homeobox transcription factor 1 beta | Nagyon gyakran (80–99%) | 1 betegségben |
| NEK8NIMA related kinase 8 | Nagyon gyakran (80–99%) | 2 betegségben |
| NPHP1nephrocystin 1 | Nagyon gyakran (80–99%) | 3 betegségben |
| NPHP3nephrocystin 3 | Nagyon gyakran (80–99%) | 1 betegségben |
| NPHP4nephrocystin 4 | Nagyon gyakran (80–99%) | 1 betegségben |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Nagyon gyakran (80–99%) | 2 betegségben |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | Nagyon gyakran (80–99%) | 2 betegségben |
| STOX1storkhead box 1 | Nagyon gyakran (80–99%) | 1 betegségben |
| WDR19WD repeat domain 19 | Nagyon gyakran (80–99%) | 1 betegségben |
| ABCB6ATP binding cassette subfamily B member 6 (LAN blood group) | Gyakran (30–79%) | 1 betegségben |
| ABCC6ATP binding cassette subfamily C member 6 | Gyakran (30–79%) | 5 betegségben |
| ABCG5ATP binding cassette subfamily G member 5 | Gyakran (30–79%) | 1 betegségben |
| ABCG8ATP binding cassette subfamily G member 8 | Gyakran (30–79%) | 1 betegségben |
| ACTA2actin alpha 2, smooth muscle | Gyakran (30–79%) | 2 betegségben |
| ADA2adenosine deaminase 2 | Gyakran (30–79%) | 3 betegségben |
| AIPAHR interacting HSP90 co-chaperone | Gyakran (30–79%) | 3 betegségben |
| ALG5ALG5 dolichyl-phosphate beta-glucosyltransferase | Gyakran (30–79%) | 2 betegségben |
| ALG9ALG9 alpha-1,2-mannosyltransferase | Gyakran (30–79%) | 1 betegségben |
| ALMS1ALMS1 centrosome and basal body associated protein | Gyakran (30–79%) | 2 betegségben |
| ANGPTL6angiopoietin like 6 | Gyakran (30–79%) | 1 betegségben |
| APOBapolipoprotein B | Gyakran (30–79%) | 1 betegségben |
| APRTadenine phosphoribosyltransferase | Gyakran (30–79%) | 1 betegségben |
| ARL6ARF like GTPase 6 | Gyakran (30–79%) | 2 betegségben |
| ARMC5armadillo repeat containing 5 | Gyakran (30–79%) | 2 betegségben |
| ASLargininosuccinate lyase | Gyakran (30–79%) | 1 betegségben |
| ATRXATRX chromatin remodeler | Gyakran (30–79%) | 1 betegségben |
| BANK1B cell scaffold protein with ankyrin repeats 1 | Gyakran (30–79%) | 1 betegségben |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Gyakran (30–79%) | 1 betegségben |
| BBIP1BBSome interacting protein 1 | Gyakran (30–79%) | 1 betegségben |
| BBS1Bardet-Biedl syndrome 1 | Gyakran (30–79%) | 2 betegségben |
| BBS10Bardet-Biedl syndrome 10 | Gyakran (30–79%) | 1 betegségben |
| BBS12Bardet-Biedl syndrome 12 | Gyakran (30–79%) | 1 betegségben |
| BBS4Bardet-Biedl syndrome 4 | Gyakran (30–79%) | 1 betegségben |
| BBS5Bardet-Biedl syndrome 5 | Gyakran (30–79%) | 1 betegségben |
| BBS7Bardet-Biedl syndrome 7 | Gyakran (30–79%) | 1 betegségben |
| BBS9Bardet-Biedl syndrome 9 | Gyakran (30–79%) | 1 betegségben |
| BICC1BicC family RNA binding protein 1 | Gyakran (30–79%) | 1 betegségben |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Gyakran (30–79%) | 1 betegségben |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Gyakran (30–79%) | 1 betegségben |
| BRCC3BRCA1/BRCA2-containing complex subunit 3 | Gyakran (30–79%) | 1 betegségben |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Gyakran (30–79%) | 1 betegségben |
| C3complement C3 | Gyakran (30–79%) | 1 betegségben |
| C4Acomplement C4A (Chido/Rodgers blood group) | Gyakran (30–79%) | 1 betegségben |
| C4Bcomplement C4B (Chido/Rodgers blood group) | Gyakran (30–79%) | 1 betegségben |
| CAV1caveolin 1 | Gyakran (30–79%) | 1 betegségben |
| CBScystathionine beta-synthase | Gyakran (30–79%) | 1 betegségben |
| CCND1cyclin D1 | Gyakran (30–79%) | 2 betegségben |
| CD46CD46 molecule | Gyakran (30–79%) | 1 betegségben |
| CDH23cadherin related 23 | Gyakran (30–79%) | 2 betegségben |
| CDKN2Acyclin dependent kinase inhibitor 2A | Gyakran (30–79%) | 1 betegségben |
| CELA2Achymotrypsin like elastase 2A | Gyakran (30–79%) | 1 betegségben |
| CEP83centrosomal protein 83 | Gyakran (30–79%) | 1 betegségben |
| CFAP418cilia and flagella associated protein 418 | Gyakran (30–79%) | 1 betegségben |
| CFBcomplement factor B | Gyakran (30–79%) | 1 betegségben |
| CFIcomplement factor I | Gyakran (30–79%) | 1 betegségben |
| CLDN16claudin 16 | Gyakran (30–79%) | 1 betegségben |
| CLIP2CAP-Gly domain containing linker protein 2 | Gyakran (30–79%) | 1 betegségben |
| COL3A1collagen type III alpha 1 chain | Gyakran (30–79%) | 2 betegségben |
| COL4A5collagen type IV alpha 5 chain | Gyakran (30–79%) | 2 betegségben |
| CR2complement C3d receptor 2 | Gyakran (30–79%) | 1 betegségben |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Gyakran (30–79%) | 2 betegségben |
| CTNNB1catenin beta 1 | Gyakran (30–79%) | 1 betegségben |
| CTSAcathepsin A | Gyakran (30–79%) | 1 betegségben |
| CTSHcathepsin H | Gyakran (30–79%) | 1 betegségben |
| DCDC2doublecortin domain containing 2 | Gyakran (30–79%) | 1 betegségben |
| DEF6DEF6 guanine nucleotide exchange factor | Gyakran (30–79%) | 1 betegségben |
| DGKEdiacylglycerol kinase epsilon | Gyakran (30–79%) | 1 betegségben |
| DLSTdihydrolipoamide S-succinyltransferase | Gyakran (30–79%) | 1 betegségben |
| DNAJB11DnaJ heat shock protein family (Hsp40) member B11 | Gyakran (30–79%) | 2 betegségben |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Gyakran (30–79%) | 1 betegségben |
| DNASE1deoxyribonuclease 1 | Gyakran (30–79%) | 1 betegségben |
| DNMT3ADNA methyltransferase 3 alpha | Gyakran (30–79%) | 1 betegségben |
| DSTdystonin | Gyakran (30–79%) | 1 betegségben |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Gyakran (30–79%) | 1 betegségben |
| EIF4Heukaryotic translation initiation factor 4H | Gyakran (30–79%) | 1 betegségben |
| ELNelastin | Gyakran (30–79%) | 4 betegségben |
| ELP1elongator acetyltransferase complex subunit 1 | Gyakran (30–79%) | 2 betegségben |
| ENGendoglin | Gyakran (30–79%) | 1 betegségben |
| ENPP1ectonucleotide pyrophosphatase/phosphodiesterase 1 | Gyakran (30–79%) | 3 betegségben |
| EPAS1endothelial PAS domain protein 1 | Gyakran (30–79%) | 1 betegségben |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Gyakran (30–79%) | 2 betegségben |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Gyakran (30–79%) | 2 betegségben |
| ETS1ETS proto-oncogene 1, transcription factor | Gyakran (30–79%) | 1 betegségben |
| EXOSC2exosome component 2 | Gyakran (30–79%) | 1 betegségben |
| FBN1fibrillin 1 | Gyakran (30–79%) | 4 betegségben |
| FCGR2BFc gamma receptor IIb | Gyakran (30–79%) | 1 betegségben |
| FCGR3BFc gamma receptor IIIb | Gyakran (30–79%) | 1 betegségben |
| FHfumarate hydratase | Gyakran (30–79%) | 1 betegségben |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Gyakran (30–79%) | 1 betegségben |
| FOXE3forkhead box E3 | Gyakran (30–79%) | 1 betegségben |
| GANABglucosidase II alpha subunit | Gyakran (30–79%) | 2 betegségben |
| GATA5GATA binding protein 5 | Gyakran (30–79%) | 1 betegségben |
| GEMIN4gem nuclear organelle associated protein 4 | Gyakran (30–79%) | 1 betegségben |
| GNASGNAS complex locus | Gyakran (30–79%) | 3 betegségben |
| GPR101G protein-coupled receptor 101 | Gyakran (30–79%) | 1 betegségben |
| GTF2Igeneral transcription factor IIi | Gyakran (30–79%) | 1 betegségben |
| GTF2IRD1GTF2I repeat domain containing 1 | Gyakran (30–79%) | 1 betegségben |
| GTF2IRD2GTF2I repeat domain containing 2 | Gyakran (30–79%) | 1 betegségben |
| H4C3H4 clustered histone 3 | Gyakran (30–79%) | 1 betegségben |
| H6PDhexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase | Gyakran (30–79%) | 1 betegségben |
| HCRThypocretin neuropeptide precursor | Gyakran (30–79%) | 1 betegségben |
| HEY2hes related family bHLH transcription factor with YRPW motif 2 | Gyakran (30–79%) | 1 betegségben |
| HLA-Bmajor histocompatibility complex, class I, B | Gyakran (30–79%) | 1 betegségben |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Gyakran (30–79%) | 1 betegségben |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Gyakran (30–79%) | 2 betegségben |
| HMBShydroxymethylbilane synthase | Gyakran (30–79%) | 2 betegségben |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Gyakran (30–79%) | 1 betegségben |
| HSD11B1hydroxysteroid 11-beta dehydrogenase 1 | Gyakran (30–79%) | 1 betegségben |
| HTRA1HtrA serine peptidase 1 | Gyakran (30–79%) | 1 betegségben |
| IDUAalpha-L-iduronidase | Gyakran (30–79%) | 1 betegségben |
| IFT172intraflagellar transport 172 | Gyakran (30–79%) | 1 betegségben |
| IFT27intraflagellar transport 27 | Gyakran (30–79%) | 1 betegségben |
| IFT74intraflagellar transport 74 | Gyakran (30–79%) | 1 betegségben |
| IGHG1immunoglobulin heavy constant gamma 1 (G1m marker) | Gyakran (30–79%) | 1 betegségben |
| IL10interleukin 10 | Gyakran (30–79%) | 1 betegségben |
| IL12Binterleukin 12B | Gyakran (30–79%) | 1 betegségben |
| IRAK1interleukin 1 receptor associated kinase 1 | Gyakran (30–79%) | 1 betegségben |
| IRF5interferon regulatory factor 5 | Gyakran (30–79%) | 1 betegségben |
| ITGAMintegrin subunit alpha M | Gyakran (30–79%) | 1 betegségben |
| JAZF1JAZF zinc finger 1 | Gyakran (30–79%) | 1 betegségben |
| KCTD1potassium channel tetramerization domain containing 1 | Gyakran (30–79%) | 2 betegségben |
| KDM1Alysine demethylase 1A | Gyakran (30–79%) | 1 betegségben |
| KIAA0319LKIAA0319 like | Gyakran (30–79%) | 1 betegségben |
| KIF1Bkinesin family member 1B | Gyakran (30–79%) | 2 betegségben |
| LDLRlow density lipoprotein receptor | Gyakran (30–79%) | 1 betegségben |
| LDLRAP1low density lipoprotein receptor adaptor protein 1 | Gyakran (30–79%) | 1 betegségben |
| LIMK1LIM domain kinase 1 | Gyakran (30–79%) | 1 betegségben |
| LIPElipase E, hormone sensitive type | Gyakran (30–79%) | 1 betegségben |
| LOXlysyl oxidase | Gyakran (30–79%) | 1 betegségben |
| LRRC8Cleucine rich repeat containing 8 VRAC subunit C | Gyakran (30–79%) | 1 betegségben |
| LZTFL1leucine zipper transcription factor like 1 | Gyakran (30–79%) | 1 betegségben |
| MAT2Amethionine adenosyltransferase 2A | Gyakran (30–79%) | 1 betegségben |
| MAXMYC associated transcriptional regulator X | Gyakran (30–79%) | 1 betegségben |
| MDH2malate dehydrogenase 2 | Gyakran (30–79%) | 1 betegségben |
| MECP2methyl-CpG binding protein 2 | Gyakran (30–79%) | 1 betegségben |
| MEF2Amyocyte enhancer factor 2A | Gyakran (30–79%) | 1 betegségben |
| METTL27methyltransferase like 27 | Gyakran (30–79%) | 1 betegségben |
| MFAP5microfibril associated protein 5 | Gyakran (30–79%) | 1 betegségben |
| MKKSMKKS centrosomal shuttling protein | Gyakran (30–79%) | 1 betegségben |
| MKS1MKS transition zone complex subunit 1 | Gyakran (30–79%) | 1 betegségben |
| MLXMAX dimerization protein MLX | Gyakran (30–79%) | 1 betegségben |
| MLXIPLMLX interacting protein like | Gyakran (30–79%) | 1 betegségben |
| MOGmyelin oligodendrocyte glycoprotein | Gyakran (30–79%) | 1 betegségben |
| MTFMTmitochondrial methionyl-tRNA formyltransferase | Gyakran (30–79%) | 1 betegségben |
| MYH11myosin heavy chain 11 | Gyakran (30–79%) | 1 betegségben |
| MYLKmyosin light chain kinase | Gyakran (30–79%) | 1 betegségben |
| NCF1neutrophil cytosolic factor 1 | Gyakran (30–79%) | 1 betegségben |
| NDUFAF6NADH:ubiquinone oxidoreductase complex assembly factor 6 | Gyakran (30–79%) | 1 betegségben |
| NF1neurofibromin 1 | Gyakran (30–79%) | 3 betegségben |
| NKX2-5NK2 homeobox 5 | Gyakran (30–79%) | 1 betegségben |
| NOTCH1notch receptor 1 | Gyakran (30–79%) | 1 betegségben |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Gyakran (30–79%) | 3 betegségben |
| OSGEPO-sialoglycoprotein endopeptidase | Gyakran (30–79%) | 1 betegségben |
| P2RY11purinergic receptor P2Y11 | Gyakran (30–79%) | 1 betegségben |
| PAX2paired box 2 | Gyakran (30–79%) | 2 betegségben |
| PBX1PBX homeobox 1 | Gyakran (30–79%) | 1 betegségben |
| PCSK9proprotein convertase subtilisin/kexin type 9 | Gyakran (30–79%) | 1 betegségben |
| PDCD1programmed cell death 1 | Gyakran (30–79%) | 1 betegségben |
| PKD1polycystin 1, transient receptor potential channel interacting | Gyakran (30–79%) | 2 betegségben |
| PKD2polycystin 2, transient receptor potential cation channel | Gyakran (30–79%) | 2 betegségben |
| PLAAT3phospholipase A and acyltransferase 3 | Gyakran (30–79%) | 1 betegségben |
| PORcytochrome p450 oxidoreductase | Gyakran (30–79%) | 2 betegségben |
| PRKG1protein kinase cGMP-dependent 1 | Gyakran (30–79%) | 1 betegségben |
| PRNPprion protein (Kanno blood group) | Gyakran (30–79%) | 1 betegségben |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Gyakran (30–79%) | 2 betegségben |
| PXKPX domain containing serine/threonine kinase like | Gyakran (30–79%) | 1 betegségben |
| RETret proto-oncogene | Gyakran (30–79%) | 3 betegségben |
| RFC2replication factor C subunit 2 | Gyakran (30–79%) | 1 betegségben |
| RNU7-1RNA, U7 small nuclear 1 | Gyakran (30–79%) | 1 betegségben |
| ROBO4roundabout guidance receptor 4 | Gyakran (30–79%) | 1 betegségben |
| SCAPERS-phase cyclin A associated protein in the ER | Gyakran (30–79%) | 1 betegségben |
| SCLT1sodium channel and clathrin linker 1 | Gyakran (30–79%) | 1 betegségben |
| SCN2Bsodium voltage-gated channel beta subunit 2 | Gyakran (30–79%) | 1 betegségben |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Gyakran (30–79%) | 2 betegségben |
| SDHAF2succinate dehydrogenase complex assembly factor 2 | Gyakran (30–79%) | 1 betegségben |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Gyakran (30–79%) | 3 betegségben |
| SDHCsuccinate dehydrogenase complex subunit C | Gyakran (30–79%) | 2 betegségben |
| SDHDsuccinate dehydrogenase complex subunit D | Gyakran (30–79%) | 2 betegségben |
| SLC16A2solute carrier family 16 member 2 | Gyakran (30–79%) | 1 betegségben |
| SLC25A11solute carrier family 25 member 11 | Gyakran (30–79%) | 2 betegségben |
| SLC35A2solute carrier family 35 member A2 | Gyakran (30–79%) | 1 betegségben |
| SMAD2SMAD family member 2 | Gyakran (30–79%) | 1 betegségben |
| SMAD3SMAD family member 3 | Gyakran (30–79%) | 1 betegségben |
| SMAD4SMAD family member 4 | Gyakran (30–79%) | 3 betegségben |
| SMAD6SMAD family member 6 | Gyakran (30–79%) | 1 betegségben |
| SPP1secreted phosphoprotein 1 | Gyakran (30–79%) | 1 betegségben |
| SPRY2sprouty RTK signaling antagonist 2 | Gyakran (30–79%) | 1 betegségben |
| STAT4signal transducer and activator of transcription 4 | Gyakran (30–79%) | 1 betegségben |
| STX1Asyntaxin 1A | Gyakran (30–79%) | 1 betegségben |
| TBL2transducin beta like 2 | Gyakran (30–79%) | 1 betegségben |
| TERTtelomerase reverse transcriptase | Gyakran (30–79%) | 1 betegségben |
| TGFB2transforming growth factor beta 2 | Gyakran (30–79%) | 1 betegségben |
| TGFB3transforming growth factor beta 3 | Gyakran (30–79%) | 1 betegségben |
| TGFBR1transforming growth factor beta receptor 1 | Gyakran (30–79%) | 1 betegségben |
| TGFBR2transforming growth factor beta receptor 2 | Gyakran (30–79%) | 1 betegségben |
| TGFBR3transforming growth factor beta receptor 3 | Gyakran (30–79%) | 1 betegségben |
| THBDthrombomodulin | Gyakran (30–79%) | 1 betegségben |
| THSD1thrombospondin type 1 domain containing 1 | Gyakran (30–79%) | 1 betegségben |
| THSD4thrombospondin type 1 domain containing 4 | Gyakran (30–79%) | 1 betegségben |
| TLR7toll like receptor 7 | Gyakran (30–79%) | 1 betegségben |
| TMEM127transmembrane protein 127 | Gyakran (30–79%) | 1 betegségben |
| TMEM237transmembrane protein 237 | Gyakran (30–79%) | 1 betegségben |
| TMEM270transmembrane protein 270 | Gyakran (30–79%) | 1 betegségben |
| TMEM67transmembrane protein 67 | Gyakran (30–79%) | 2 betegségben |
| TNFAIP3TNF alpha induced protein 3 | Gyakran (30–79%) | 1 betegségben |
| TNFRSF11ATNF receptor superfamily member 11a | Gyakran (30–79%) | 1 betegségben |
| TNFRSF11BTNF receptor superfamily member 11b | Gyakran (30–79%) | 1 betegségben |
| TNFSF4TNF superfamily member 4 | Gyakran (30–79%) | 2 betegségben |
| TNIP1TNFAIP3 interacting protein 1 | Gyakran (30–79%) | 1 betegségben |
| TP53tumor protein p53 | Gyakran (30–79%) | 2 betegségben |
| TREX1three prime repair exonuclease 1 | Gyakran (30–79%) | 2 betegségben |
| TRIM32tripartite motif containing 32 | Gyakran (30–79%) | 1 betegségben |
| TTC8tetratricopeptide repeat domain 8 | Gyakran (30–79%) | 1 betegségben |
| UBE2L3ubiquitin conjugating enzyme E2 L3 | Gyakran (30–79%) | 1 betegségben |
| UMODuromodulin | Gyakran (30–79%) | 1 betegségben |
| USP48ubiquitin specific peptidase 48 | Gyakran (30–79%) | 1 betegségben |
| USP8ubiquitin specific peptidase 8 | Gyakran (30–79%) | 2 betegségben |
| VHLvon Hippel-Lindau tumor suppressor | Gyakran (30–79%) | 4 betegségben |
| VPS37DVPS37D subunit of ESCRT-I | Gyakran (30–79%) | 1 betegségben |
| WDPCPWD repeat containing planar cell polarity effector | Gyakran (30–79%) | 1 betegségben |
| WT1WT1 transcription factor | Gyakran (30–79%) | 4 betegségben |
| XPNPEP3X-prolyl aminopeptidase 3 | Gyakran (30–79%) | 1 betegségben |
| YY1AP1YY1 associated protein 1 | Gyakran (30–79%) | 1 betegségben |
| ZNF365zinc finger protein 365 | Gyakran (30–79%) | 1 betegségben |
| ZNRF3zinc and ring finger 3 | Gyakran (30–79%) | 1 betegségben |
| ABCB4ATP binding cassette subfamily B member 4 | Néha (5–29%) | 1 betegségben |
| ACAT1acetyl-CoA acetyltransferase 1 | Néha (5–29%) | 1 betegségben |
| ACP5acid phosphatase 5, tartrate resistant | Néha (5–29%) | 1 betegségben |
| ADAMTSL4ADAMTS like 4 | Néha (5–29%) | 1 betegségben |
| ALKALK receptor tyrosine kinase | Néha (5–29%) | 2 betegségben |
| ALX4ALX homeobox 4 | Néha (5–29%) | 1 betegségben |
| ARHGEF15Rho guanine nucleotide exchange factor 15 | Néha (5–29%) | 1 betegségben |
| BNC2basonuclin zinc finger protein 2 | Néha (5–29%) | 1 betegségben |
| BRCA2BRCA2 DNA repair associated | Néha (5–29%) | 1 betegségben |
| BSCL2BSCL2 lipid droplet biogenesis associated, seipin | Néha (5–29%) | 1 betegségben |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Néha (5–29%) | 1 betegségben |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Néha (5–29%) | 1 betegségben |
| CMPK2cytidine/uridine monophosphate kinase 2 | Néha (5–29%) | 1 betegségben |
| CTR9CTR9 component of Paf1/RNA polymerase II complex | Néha (5–29%) | 1 betegségben |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Néha (5–29%) | 1 betegségben |
| EDAectodysplasin A | Néha (5–29%) | 1 betegségben |
| EDA2Rectodysplasin A2 receptor | Néha (5–29%) | 1 betegségben |
| EMILIN1elastin microfibril interfacer 1 | Néha (5–29%) | 1 betegségben |
| EXT2exostosin glycosyltransferase 2 | Néha (5–29%) | 1 betegségben |
| FIG4FIG4 phosphoinositide 5-phosphatase | Néha (5–29%) | 1 betegségben |
| FMR1fragile X messenger ribonucleoprotein 1 | Néha (5–29%) | 1 betegségben |
| FUZfuzzy planar cell polarity protein | Néha (5–29%) | 1 betegségben |
| GCH1GTP cyclohydrolase 1 | Néha (5–29%) | 1 betegségben |
| GLAgalactosidase alpha | Néha (5–29%) | 2 betegségben |
| GPC3glypican 3 | Néha (5–29%) | 1 betegségben |
| H19H19 imprinted maternally expressed transcript | Néha (5–29%) | 1 betegségben |
| HGDhomogentisate 1,2-dioxygenase | Néha (5–29%) | 1 betegségben |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Néha (5–29%) | 1 betegségben |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Néha (5–29%) | 1 betegségben |
| HPSE2heparanase 2 (inactive) | Néha (5–29%) | 1 betegségben |
| HRHR lysine demethylase and nuclear receptor corepressor | Néha (5–29%) | 1 betegségben |
| IFIH1interferon induced with helicase C domain 1 | Néha (5–29%) | 1 betegségben |
| IFNGinterferon gamma | Néha (5–29%) | 1 betegségben |
| IMPDH2inosine monophosphate dehydrogenase 2 | Néha (5–29%) | 1 betegségben |
| JAM2junctional adhesion molecule 2 | Néha (5–29%) | 1 betegségben |
| LAMB1laminin subunit beta 1 | Néha (5–29%) | 1 betegségben |
| LEMD3LEM domain containing 3 | Néha (5–29%) | 1 betegségben |
| LRIG2leucine rich repeats and immunoglobulin like domains 2 | Néha (5–29%) | 1 betegségben |
| LRPPRCleucine rich pentatricopeptide repeat containing | Néha (5–29%) | 1 betegségben |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Néha (5–29%) | 1 betegségben |
| MC4Rmelanocortin 4 receptor | Néha (5–29%) | 1 betegségben |
| MED12mediator complex subunit 12 | Néha (5–29%) | 1 betegségben |
| MEN1menin 1 | Néha (5–29%) | 1 betegségben |
| MMP14matrix metallopeptidase 14 | Néha (5–29%) | 1 betegségben |
| MMP2matrix metallopeptidase 2 | Néha (5–29%) | 1 betegségben |
| MT-TKmitochondrially encoded tRNA-Lys (AAA/G) | Néha (5–29%) | 2 betegségben |
| MTRR5-methyltetrahydrofolate-homocysteine methyltransferase reductase | Néha (5–29%) | 1 betegségben |
| MYORGmyogenesis regulating glycosidase | Néha (5–29%) | 1 betegségben |
| NAA60N-alpha-acetyltransferase 60, NatF catalytic subunit | Néha (5–29%) | 1 betegségben |
| NOD2nucleotide binding oligomerization domain containing 2 | Néha (5–29%) | 2 betegségben |
| NOTCH3notch receptor 3 | Néha (5–29%) | 2 betegségben |
| NR4A2nuclear receptor subfamily 4 group A member 2 | Néha (5–29%) | 1 betegségben |
| OFD1OFD1 centriole and centriolar satellite protein | Néha (5–29%) | 2 betegségben |
| PDE11Aphosphodiesterase 11A | Néha (5–29%) | 2 betegségben |
| PDGFBplatelet derived growth factor subunit B | Néha (5–29%) | 1 betegségben |
| PDGFRBplatelet derived growth factor receptor beta | Néha (5–29%) | 1 betegségben |
| PHF21APHD finger protein 21A | Néha (5–29%) | 1 betegségben |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Néha (5–29%) | 1 betegségben |
| POU3F4POU class 3 homeobox 4 | Néha (5–29%) | 1 betegségben |
| POU6F2POU class 6 homeobox 2 | Néha (5–29%) | 1 betegségben |
| PPOXprotoporphyrinogen oxidase | Néha (5–29%) | 1 betegségben |
| PRTN3proteinase 3 | Néha (5–29%) | 1 betegségben |
| RESTRE1 silencing transcription factor | Néha (5–29%) | 1 betegségben |
| RNU4ATACRNA, U4atac small nuclear | Néha (5–29%) | 1 betegségben |
| RRP12ribosomal RNA processing 12 homolog | Néha (5–29%) | 1 betegségben |
| SLC20A2solute carrier family 20 member 2 | Néha (5–29%) | 1 betegségben |
| SLC2A10solute carrier family 2 member 10 | Néha (5–29%) | 2 betegségben |
| SLC37A4solute carrier family 37 member 4 | Néha (5–29%) | 3 betegségben |
| SLC7A7solute carrier family 7 member 7 | Néha (5–29%) | 1 betegségben |
| TRIM28tripartite motif containing 28 | Néha (5–29%) | 1 betegségben |
| TRIP13thyroid hormone receptor interactor 13 | Néha (5–29%) | 1 betegségben |
| TSC1TSC complex subunit 1 | Néha (5–29%) | 1 betegségben |
| TSC2TSC complex subunit 2 | Néha (5–29%) | 1 betegségben |
| VAC14VAC14 component of PIKFYVE complex | Néha (5–29%) | 1 betegségben |
| VANGL1VANGL planar cell polarity protein 1 | Néha (5–29%) | 1 betegségben |
| WRNWRN RecQ like helicase | Néha (5–29%) | 1 betegségben |
| XPR1xenotropic and polytropic retrovirus receptor 1 | Néha (5–29%) | 1 betegségben |
| XYLT1xylosyltransferase 1 | Néha (5–29%) | 1 betegségben |
| XYLT2xylosyltransferase 2 | Néha (5–29%) | 1 betegségben |
| ZFXzinc finger protein X-linked | Néha (5–29%) | 1 betegségben |
| ZMPSTE24zinc metallopeptidase STE24 | Néha (5–29%) | 1 betegségben |
| ACBD6acyl-CoA binding domain containing 6 | Ritkán (1–4%) | 1 betegségben |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Ritkán (1–4%) | 1 betegségben |
| LIN28Blin-28 RNA binding posttranscriptional regulator B | Ritkán (1–4%) | 1 betegségben |
| LMO1LIM domain only 1 | Ritkán (1–4%) | 1 betegségben |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Ritkán (1–4%) | 1 betegségben |
| PHOX2Bpaired like homeobox 2B | Ritkán (1–4%) | 1 betegségben |
| ACVRL1activin A receptor like type 1 | Nincs rögzítve | 1 betegségben |
| ARHGAP31Rho GTPase activating protein 31 | Nincs rögzítve | 1 betegségben |
| BMPR2bone morphogenetic protein receptor type 2 | Nincs rögzítve | 1 betegségben |
| BSNDbarttin CLCNK type accessory subunit beta | Nincs rögzítve | 1 betegségben |
| CCDC28Bcoiled-coil domain containing 28B | Nincs rögzítve | 1 betegségben |
| CD2APCD2 associated protein | Nincs rögzítve | 1 betegségben |
| CFHcomplement factor H | Nincs rögzítve | 1 betegségben |
| CFHR1complement factor H related 1 | Nincs rögzítve | 1 betegségben |
| CFHR3complement factor H related 3 | Nincs rögzítve | 1 betegségben |
| CLCNKAchloride voltage-gated channel Ka | Nincs rögzítve | 1 betegségben |
| CLCNKBchloride voltage-gated channel Kb | Nincs rögzítve | 1 betegségben |
| COL4A3collagen type IV alpha 3 chain | Nincs rögzítve | 2 betegségben |
| COL4A4collagen type IV alpha 4 chain | Nincs rögzítve | 2 betegségben |
| COQ7coenzyme Q7, hydroxylase | Nincs rögzítve | 1 betegségben |
| CPOXcoproporphyrinogen oxidase | Nincs rögzítve | 1 betegségben |
| CUL3cullin 3 | Nincs rögzítve | 1 betegségben |
| CYP21A2cytochrome P450 family 21 subfamily A member 2 | Nincs rögzítve | 1 betegségben |
| EPORerythropoietin receptor | Nincs rögzítve | 1 betegségben |
| FGAfibrinogen alpha chain | Nincs rögzítve | 1 betegségben |
| FMO3flavin containing dimethylaniline monoxygenase 3 | Nincs rögzítve | 1 betegségben |
| G6PC1glucose-6-phosphatase catalytic subunit 1 | Nincs rögzítve | 1 betegségben |
| GBA1glucosylceramidase beta 1 | Nincs rögzítve | 1 betegségben |
| HBBhemoglobin subunit beta | Nincs rögzítve | 1 betegségben |
| INF2inverted formin 2 | Nincs rögzítve | 1 betegségben |
| ITGA8integrin subunit alpha 8 | Nincs rögzítve | 1 betegségben |
| KLHL3kelch like family member 3 | Nincs rögzítve | 1 betegségben |
| KRT18keratin 18 | Nincs rögzítve | 1 betegségben |
| LARS2leucyl-tRNA synthetase 2, mitochondrial | Nincs rögzítve | 1 betegségben |
| LRP6LDL receptor related protein 6 | Nincs rögzítve | 1 betegségben |
| MGPmatrix Gla protein | Nincs rögzítve | 1 betegségben |
| MT-CO1mitochondrially encoded cytochrome c oxidase I | Nincs rögzítve | 1 betegségben |
| MT-CO2mitochondrially encoded cytochrome c oxidase II | Nincs rögzítve | 1 betegségben |
| MT-CO3mitochondrially encoded cytochrome c oxidase III | Nincs rögzítve | 1 betegségben |
| MT-CYBmitochondrially encoded cytochrome b | Nincs rögzítve | 1 betegségben |
| MT-ND1mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 1 | Nincs rögzítve | 1 betegségben |
| MT-ND5mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 5 | Nincs rögzítve | 1 betegségben |
| MT-ND6mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 6 | Nincs rögzítve | 1 betegségben |
| MT-TCmitochondrially encoded tRNA-Cys (UGU/C) | Nincs rögzítve | 1 betegségben |
| MT-TFmitochondrially encoded tRNA-Phe (UUU/C) | Nincs rögzítve | 1 betegségben |
| MT-THmitochondrially encoded tRNA-His (CAU/C) | Nincs rögzítve | 1 betegségben |
| MT-TL1mitochondrially encoded tRNA-Leu (UUA/G) 1 | Nincs rögzítve | 1 betegségben |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | Nincs rögzítve | 1 betegségben |
| MT-TQmitochondrially encoded tRNA-Gln (CAA/G) | Nincs rögzítve | 1 betegségben |
| MT-TS1mitochondrially encoded tRNA-Ser (UCN) 1 | Nincs rögzítve | 1 betegségben |
| MT-TS2mitochondrially encoded tRNA-Ser (AGU/C) 2 | Nincs rögzítve | 1 betegségben |
| MT-TVmitochondrially encoded tRNA-Val (GUN) | Nincs rögzítve | 1 betegségben |
| MT-TWmitochondrially encoded tRNA-Trp (UGA/G) | Nincs rögzítve | 1 betegségben |
| MUC1mucin 1, cell surface associated | Nincs rögzítve | 1 betegségben |
| NFIXnuclear factor I X | Nincs rögzítve | 1 betegségben |
| NOTCH2notch receptor 2 | Nincs rögzítve | 1 betegségben |
| NR3C2nuclear receptor subfamily 3 group C member 2 | Nincs rögzítve | 1 betegségben |
| NSMCE2NSE2 SUMO ligase component of SMC5/6 complex | Nincs rögzítve | 1 betegségben |
| PAM16presequence translocase associated motor 16 | Nincs rögzítve | 1 betegségben |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Nincs rögzítve | 1 betegségben |
| SERPINA6serpin family A member 6 | Nincs rögzítve | 1 betegségben |
| SH2B3SH2B adaptor protein 3 | Nincs rögzítve | 1 betegségben |
| STAT2signal transducer and activator of transcription 2 | Nincs rögzítve | 1 betegségben |
| SUGCTsuccinyl-CoA:glutarate-CoA transferase | Nincs rögzítve | 1 betegségben |
| TMEM70transmembrane protein 70 | Nincs rögzítve | 1 betegségben |
| TRPC6transient receptor potential cation channel subfamily C member 6 | Nincs rögzítve | 1 betegségben |
| WDR35WD repeat domain 35 | Nincs rögzítve | 1 betegségben |
| WNK4WNK lysine deficient protein kinase 4 | 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.
Szűkebb tulajdonságok
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: 2026.10.19-9814e911.
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