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Merkmal
Abdominal pain
An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) and perceived to originate in the abdomen.
Zusammenfassung
- Auch genannt
- Abdominal discomfort, Gastro pain, Gastrointestinal pain, Pain in stomach, Stomach pain, Upset stomach
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Meinen Genome Test bestellen170 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.
- Nephrotic SyndromeReads 19 of these genesACTN4ARHGDIACOQ8BDAAM2EMP2KANK2About this report →
- Focal Segmental GlomerulosclerosisReads 9 of these genesACTN4ANLNAPOL1CD2APCRB2INF2About this report →
- GlomerulosclerosisReads 7 of these genesACTN4ANLNCRB2INF2MYO1EPAX2About this report →
- Lynch SyndromeReads 5 of these genesEPCAMMLH1MSH2MSH6PMS2About this report →
Show 166 more reports
- PancreatitisReads 5 of these genesCPA1CTRCPRSS1TRPV6SPINK1About this report →
- Malignant Endocrine NeoplasmReads 6 of these genesRETSDHASDHBTP53CDKN1BMEN1About this report →
- Red Blood Cell Membrane DisordersReads 6 of these genesKCNN4PIEZO1SLC4A1SPTA1SPTBEPB41About this report →
- Hereditary SpherocytosisReads 5 of these genesANK1EPB42SLC4A1SPTA1SPTBAbout this report →
- Urinary and Renal System TumourReads 7 of these genesMETRETSDHASDHBTP53TRIM28About this report →
- Polycystic Liver Disease (1 and 2)Reads 4 of these genesALG8LRP5PRKCSHSEC63About this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 6 of these genesRETSDHASDHBSDHCSDHDVHLAbout this report →
- Kidney CancerReads 5 of these genesMETSDHBTP53TRIM28VHLAbout this report →
- Hereditary Periodic Fever SyndromesReads 4 of these genesMVKTNFRSF1ANLRP3NLRP12About this report →
- Other Inborn Errors of ImmunityReads 23 of these genesIRF4NCF4PIK3CGATMKRASNCF1About this report →
- Autoimmune DiseaseReads 7 of these genesKRASCTLA4DNASE1L3FASNOD2SAT1About this report →
- Colorectal Cancer & PolyposisReads 4 of these genesMUTYHPOLD1POLEAPCAbout this report →
- Waardenburg SyndromeReads 4 of these genesEDN3EDNRBSOX10MITFAbout this report →
- Hereditary Gastrointestinal Stromal TumourReads 3 of these genesSDHBSDHCKITAbout this report →
- Hepatic Porphyria DisordersReads 4 of these genesPPOXCPOXHMBSALADAbout this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Hereditary Wilms TumourReads 2 of these genesWT1RESTAbout this report →
- Juvenile Polyposis SyndromeReads 2 of these genesBMPR1ASMAD4About this report →
- Myotonic DystrophyReads 2 of these genesCNBPDMPKAbout this report →
- Tuberous SclerosisReads 2 of these genesTSC1TSC2About this report →
- ThalassaemiaReads 3 of these genesHBBHBG1HBG2About this report →
- PorphyriaReads 4 of these genesPPOXCPOXHMBSALADAbout this report →
- Familial Intrahepatic CholestasisReads 4 of these genesABCB11ABCB4ATP8B1NR1H4About this report →
- Disorder of Copper MetabolismReads 2 of these genesATP7AATP7BAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 3 of these genesKRASCTLA4FASAbout this report →
- Thyroid CancerReads 6 of these genesCASRRETTRPV6GNA11MEN1NKX2-5About this report →
- DNA Repair DiseaseReads 7 of these genesBRCA1BRCA2MLH1MSH2MSH6PALB2About this report →
- PolycythemiaReads 3 of these genesEPORHBBVHLAbout this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 3 of these genesATMCHEK2PALB2About this report →
- Hemolytic Uremic Syndrome, Interstitial NephritisReads 3 of these genesCD46CFHCFIAbout this report →
- MelanomaReads 2 of these genesCDKN2AMITFAbout this report →
- Acid Sphingomyelinase Deficiency (Niemann-Pick Disease Types A and B)Reads 1 of these genesSMPD1About this report →
- Ataxia-TelangiectasiaReads 1 of these genesATMAbout this report →
- Brugada SyndromeReads 1 of these genesSCN5AAbout this report →
- CHAPLE Disease (CD55 Deficiency)Reads 1 of these genesCD55About this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- Curry-Jones Syndrome (Mosaic SMO Syndrome)Reads 1 of these genesSMOAbout this report →
- Cystic FibrosisReads 1 of these genesCFTRAbout this report →
- Deficiency of Adenosine Deaminase 2 (DADA2)Reads 1 of these genesADA2About this report →
- Dias-Logan SyndromeReads 1 of these genesBCL11AAbout this report →
- Fabry DiseaseReads 1 of these genesGLAAbout this report →
- Familial Mediterranean FeverReads 1 of these genesMEFVAbout this report →
- FDXR-Related Mitochondrial DisorderReads 1 of these genesFDXRAbout this report →
- Focal Dermal Hypoplasia (Goltz Syndrome)Reads 1 of these genesPORCNAbout this report →
- G6PD DeficiencyReads 1 of these genesG6PDAbout this report →
- Gaucher DiseaseReads 1 of these genesGBA1About this report →
- Gitelman SyndromeReads 1 of these genesSLC12A3About this report →
- Hereditary Thrombocythaemia (JAK2)Reads 1 of these genesJAK2About this report →
- Hyperprolinaemia Type 2Reads 1 of these genesALDH4A1About this report →
- LAMA5-Related Multisystemic SyndromeReads 1 of these genesLAMA5About this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- Low phospholipid-associated cholelithiasisReads 1 of these genesABCB4About this report →
- MDPL SyndromeReads 1 of these genesPOLD1About this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- Perlman SyndromeReads 1 of these genesDIS3L2About this report →
- Peutz-Jeghers SyndromeReads 1 of these genesSTK11About this report →
- Polycystic Ovary SyndromeReads 1 of these genesFSHRAbout this report →
- Polyglucosan Body Myopathy 1 (RBCK1)Reads 1 of these genesRBCK1About this report →
- Sickle Cell DiseaseReads 1 of these genesHBBAbout this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
- Von Hippel-Lindau DiseaseReads 1 of these genesVHLAbout this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- X-Linked Adrenoleukodystrophy (ABCD1)Reads 1 of these genesABCD1About this report →
- Severe Congenital NeutropeniaReads 3 of these genesCLPBELANEGFI1About this report →
- Chronic Granulomatous DiseaseReads 2 of these genesNCF4NCF1About this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 2 of these genesGHSRSTAT5BAbout this report →
- HemochromatosisReads 2 of these genesHFETFR2About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 2 of these genesERBB3ACTG2About this report →
- Systemic Lupus ErythematosusReads 2 of these genesDNASE1L3SAT1About this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 2 of these genesCASRGNA11About this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 2 of these genesRUNX1TERTAbout this report →
- Fanconi AnemiaReads 3 of these genesBRCA1BRCA2PALB2About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 2 of these genesSCN5ATRPM4About this report →
- Age-Related Macular DegenerationReads 1 of these genesCFHAbout this report →
- Congenital Disaccharidase DeficienciesReads 1 of these genesSIAbout this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesPTENAbout this report →
- Gilbert SyndromeReads 1 of these genesABCC2About this report →
- Hereditary Gingival FibromatosisReads 1 of these genesRESTAbout this report →
- Hereditary Mixed Polyposis SyndromeReads 1 of these genesBMPR1AAbout this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 4 of these genesLYNELF4OTULINADA2About this report →
- Intellectual DisabilityReads 10 of these genesCASKCTNNB1SMAD4ASXL1MED12FGF13About this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 2 of these genesIKZF1IRF2BP2About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 2 of these genesIFNGR1IL23RAbout this report →
- Familial HypomagnesemiaReads 2 of these genesTRPV6CLDN16About this report →
- Polycystic Kidney DiseaseReads 2 of these genesPKHD1ALG8About this report →
- Primary Mitochondrial DiseaseReads 7 of these genesGUK1DNAJC30LIG3POLGRRM2BTYMPAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 9 of these genesFDXRATP7ALIG3POLGRRM2BSDHAAbout this report →
- Alport SyndromeReads 1 of these genesCOL4A3About this report →
- Hereditary AngioedemaReads 1 of these genesSERPING1About this report →
- Hereditary Fructose Intolerance & Gluconeogenesis DefectsReads 1 of these genesALDOBAbout this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesRETAbout this report →
- Tetralogy of FallotReads 1 of these genesNKX2-5About this report →
- Congenital Diarrhoeas & EnteropathiesReads 2 of these genesEPCAMGUCY2CAbout this report →
- Inherited Congenital Heart DefectsReads 2 of these genesELNNKX2-5About this report →
- Female InfertilityReads 4 of these genesATMFSHRTRIP13NUP107About this report →
- OsteopetrosisReads 2 of these genesTCIRG1LRP5About this report →
- Cutis LaxaReads 2 of these genesATP7AELNAbout this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Congenital Dyserythropoietic AnaemiasReads 1 of these genesKLF1About this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- PorokeratosisReads 1 of these genesMVKAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesPRKAR1AAbout this report →
- Inherited Complement and Properdin DeficienciesReads 2 of these genesC4ACFIAbout this report →
- GPI Anchor Biosynthesis DefectsReads 2 of these genesPIGTPIGYAbout this report →
- Bartter DiseaseReads 1 of these genesCLCNKBAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 1 of these genesHBBAbout this report →
- Mosaic Variegated Aneuploidy SyndromeReads 1 of these genesTRIP13About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesLRP5About this report →
- Noonan SyndromeReads 2 of these genesKRASCBLAbout this report →
- Dyskeratosis CongenitaReads 2 of these genesTERTNPM1About this report →
- Inherited Neurodegenerative DisordersReads 8 of these genesABCD1ATMATP7APOLGSDHAFUSAbout this report →
- Cornelia de Lange SyndromeReads 1 of these genesRAD21About this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesIL10About this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFBR2About this report →
- Renal Tubular AcidosisReads 1 of these genesSLC4A1About this report →
- Syndromic and Metabolic CardiomyopathiesReads 1 of these genesNKX2-5About this report →
- Congenital Disorders of GlycosylationReads 4 of these genesPIGTPIGYALG8POMT1About this report →
- Lysosomal Storage DiseaseReads 3 of these genesGLAGBA1SMPD1About this report →
- VitreoretinopathyReads 2 of these genesCTNNB1LRP5About this report →
- Hypertrophic CardiomyopathyReads 3 of these genesKRASH19DMPKAbout this report →
- Classic Organic AciduriasReads 1 of these genesMLYCDAbout this report →
- Hereditary HypolipoproteinemiasReads 1 of these genesABCA1About this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT3About this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesCTLA4About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 2 of these genesFUSTBK1About this report →
- Purine & Pyrimidine Metabolism DisordersReads 1 of these genesAPRTAbout 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 genesF5About this report →
- Long QT SyndromeReads 1 of these genesSCN5AAbout this report →
- Marfan Like SyndromesReads 1 of these genesTGFBR2About this report →
- Rare Inherited Coagulation Factor DeficienciesReads 1 of these genesF5About this report →
- Male InfertilityReads 2 of these genesFKBP6CFTRAbout this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 1 of these genesPAX2About this report →
- Hermansky-Pudlak SyndromeReads 1 of these genesHPS1About this report →
- Epilepsy (Full Panel)Reads 4 of these genesGOSR2SCARB2SCN1BFGF13About this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesCELAbout this report →
- Urea Cycle DisorderReads 1 of these genesOTCAbout this report →
- Aortic AneurysmReads 1 of these genesTGFBR2About this report →
- Frontotemporal DementiaReads 1 of these genesTBK1About this report →
- HyperlipidemiaReads 1 of these genesABCG8About this report →
- Methylmalonic & Propionic AcidemiaReads 1 of these genesMMUTAbout this report →
- Parkinson DiseaseReads 1 of these genesGBA1About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesPIEZO1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesWT1About this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesATP7AINF2About this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-5About this report →
- Syndromic CraniosynostosisReads 1 of these genesSMOAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesSMOAbout this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Spinal Muscular AtrophyReads 1 of these genesATP7AAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesPOMT1About this report →
- Diabetes MellitusReads 1 of these genesCELAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesRUNX1About this report →
- Osteogenesis ImperfectaReads 1 of these genesLRP5About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 1 of these genesTRPM4About this report →
- Dilated CardiomyopathyReads 1 of these genesSCN5AAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesRNF168About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesABCD1About this report →
- Leigh SyndromeReads 1 of these genesSDHAAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesABCD1About this report →
- Hearing Loss and DeafnessReads 1 of these genesMETAbout this report →
Lesen Sie die Gene aus, die mit Abdominal pain zusammenhängen, und den Rest Ihres Genoms, mit einem einzigen Test.
Ab 449 $Kostenloser Versand · Ergebnisse in 6–8 Wochen
Meinen Genome Test bestellen327 Gene mit Abdominal pain verknüpft
Veränderungen in diesen Genen verursachen seltene Erkrankungen, bei denen Abdominal pain auftritt. Die meisten Menschen mit diesem Merkmal haben keine dieser Erkrankungen, und ein Gen auf dieser Liste sagt nichts über das eigene Genom einer Person aus.
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| ABCB1ATP binding cassette subfamily B member 1 | Immer | In 1 Erkrankung |
| APRTadenine phosphoribosyltransferase | Immer | In 1 Erkrankung |
| CARD8caspase recruitment domain family member 8 | Immer | In 1 Erkrankung |
| CASKcalcium/calmodulin dependent serine protein kinase | Immer | In 1 Erkrankung |
| CEBPECCAAT enhancer binding protein epsilon | Immer | In 1 Erkrankung |
| FDXRferredoxin reductase | Immer | In 1 Erkrankung |
| G6PDglucose-6-phosphate dehydrogenase | Immer | In 1 Erkrankung |
| GUK1guanylate kinase 1 | Immer | In 1 Erkrankung |
| IRF4interferon regulatory factor 4 | Immer | In 2 Erkrankungen |
| LYNLYN proto-oncogene, Src family tyrosine kinase | Immer | In 1 Erkrankung |
| NCF4neutrophil cytosolic factor 4 | Immer | In 1 Erkrankung |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Immer | In 1 Erkrankung |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Immer | In 1 Erkrankung |
| PIK3CGphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma | Immer | In 1 Erkrankung |
| PLD4phospholipase D family member 4 | Immer | In 1 Erkrankung |
| PPOXprotoporphyrinogen oxidase | Immer | In 2 Erkrankungen |
| RAD21RAD21 cohesin complex component | Immer | In 1 Erkrankung |
| RNU6ATACRNA, U6atac small nuclear | Immer | In 1 Erkrankung |
| STK11serine/threonine kinase 11 | Immer | In 2 Erkrankungen |
| TRU-TCA1-1tRNA-SeC (anticodon TCA) 1-1 | Immer | In 1 Erkrankung |
| ABCD1ATP binding cassette subfamily D member 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ALDOBaldolase, fructose-bisphosphate B | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| ATMATM serine/threonine kinase | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ATP7AATPase copper transporting alpha | Sehr häufig (80–99 %) | In 1 Erkrankung |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Sehr häufig (80–99 %) | In 1 Erkrankung |
| BMPR1Abone morphogenetic protein receptor type 1A | Sehr häufig (80–99 %) | In 3 Erkrankungen |
| BRCA1BRCA1 DNA repair associated | Sehr häufig (80–99 %) | In 3 Erkrankungen |
| BRCA2BRCA2 DNA repair associated | Sehr häufig (80–99 %) | In 4 Erkrankungen |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Sehr häufig (80–99 %) | In 1 Erkrankung |
| CASRcalcium sensing receptor | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| CD4CD4 molecule | Sehr häufig (80–99 %) | In 1 Erkrankung |
| CDKN2Acyclin dependent kinase inhibitor 2A | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| CHEK2checkpoint kinase 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| CLIP2CAP-Gly domain containing linker protein 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| CPA1carboxypeptidase A1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| CPOXcoproporphyrinogen oxidase | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| CTNNB1catenin beta 1 | Sehr häufig (80–99 %) | In 3 Erkrankungen |
| CTRCchymotrypsin C | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ECE1endothelin converting enzyme 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
287 weitere Gene anzeigen
| Gen | Wie häufig es auftritt | Erkrankungen |
|---|---|---|
| EDN3endothelin 3 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| EDNRBendothelin receptor type B | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| EIF4Heukaryotic translation initiation factor 4H | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ELNelastin | Sehr häufig (80–99 %) | In 1 Erkrankung |
| EPCAMepithelial cell adhesion molecule | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ERBB2erb-b2 receptor tyrosine kinase 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| ERBB3erb-b2 receptor tyrosine kinase 3 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| EWSR1EWS RNA binding protein 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Sehr häufig (80–99 %) | In 1 Erkrankung |
| FSHRfollicle stimulating hormone receptor | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| GDNFglial cell derived neurotrophic factor | Sehr häufig (80–99 %) | In 1 Erkrankung |
| GHSRgrowth hormone secretagogue receptor | Sehr häufig (80–99 %) | In 1 Erkrankung |
| GLAgalactosidase alpha | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| GTF2Igeneral transcription factor IIi | Sehr häufig (80–99 %) | In 1 Erkrankung |
| GTF2IRD1GTF2I repeat domain containing 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| GTF2IRD2GTF2I repeat domain containing 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| HMBShydroxymethylbilane synthase | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| JAK2Janus kinase 2 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| KRASKRas proto-oncogene, GTPase | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| LIG3DNA ligase 3 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| LIMK1LIM domain kinase 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| MEFVMEFV innate immunity regulator, pyrin | Sehr häufig (80–99 %) | In 4 Erkrankungen |
| METMET proto-oncogene, receptor tyrosine kinase | Sehr häufig (80–99 %) | In 1 Erkrankung |
| METTL27methyltransferase like 27 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| MLH1mutL homolog 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| MSH2mutS homolog 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| MSH6mutS homolog 6 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| MUTYHmutY DNA glycosylase | Sehr häufig (80–99 %) | In 1 Erkrankung |
| MVKmevalonate kinase | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| NCF1neutrophil cytosolic factor 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| NPATnuclear protein, coactivator of histone transcription | Sehr häufig (80–99 %) | In 1 Erkrankung |
| NRTNneurturin | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PALB2partner and localizer of BRCA2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PALLDpalladin, cytoskeletal associated protein | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PMS1PMS1 homolog 1, mismatch repair system component | Sehr häufig (80–99 %) | In 1 Erkrankung |
| PMS2PMS1 homolog 2, mismatch repair system component | Sehr häufig (80–99 %) | In 1 Erkrankung |
| POLD1DNA polymerase delta 1, catalytic subunit | Sehr häufig (80–99 %) | In 1 Erkrankung |
| POLEDNA polymerase epsilon, catalytic subunit | Sehr häufig (80–99 %) | In 1 Erkrankung |
| POLGDNA polymerase gamma, catalytic subunit | Sehr häufig (80–99 %) | In 3 Erkrankungen |
| PRSS1serine protease 1 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| PRSS2serine protease 2 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| RABL3RAB, member of RAS oncogene family like 3 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| RETret proto-oncogene | Sehr häufig (80–99 %) | In 1 Erkrankung |
| RFC2replication factor C subunit 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| RPS20ribosomal protein S20 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| RRM2Bribonucleotide reductase regulatory TP53 inducible subunit M2B | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SDHAsuccinate dehydrogenase complex flavoprotein subunit A | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| SDHBsuccinate dehydrogenase complex iron sulfur subunit B | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| SDHCsuccinate dehydrogenase complex subunit C | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| SEMA3Csemaphorin 3C | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SEMA3Dsemaphorin 3D | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SEMA4Asemaphorin 4A | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SERPING1serpin family G member 1 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| SIsucrase-isomaltase | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| SMAD4SMAD family member 4 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| SMOsmoothened, frizzled class receptor | Sehr häufig (80–99 %) | In 1 Erkrankung |
| SOX10SRY-box transcription factor 10 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| SREBF1sterol regulatory element binding transcription factor 1 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| STX1Asyntaxin 1A | Sehr häufig (80–99 %) | In 1 Erkrankung |
| TBL2transducin beta like 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| TGFBR2transforming growth factor beta receptor 2 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| TMEM270transmembrane protein 270 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| TNFRSF1ATNF receptor superfamily member 1A | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| TP53tumor protein p53 | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| TRPV6transient receptor potential cation channel subfamily V member 6 | Sehr häufig (80–99 %) | In 1 Erkrankung |
| TYMPthymidine phosphorylase | Sehr häufig (80–99 %) | In 2 Erkrankungen |
| VPS37DVPS37D subunit of ESCRT-I | Sehr häufig (80–99 %) | In 1 Erkrankung |
| WT1WT1 transcription factor | Sehr häufig (80–99 %) | In 3 Erkrankungen |
| ABCA1ATP binding cassette subfamily A member 1 | Häufig (30–79 %) | In 1 Erkrankung |
| ALADaminolevulinate dehydratase | Häufig (30–79 %) | In 1 Erkrankung |
| APCAPC regulator of Wnt signaling pathway | Häufig (30–79 %) | In 2 Erkrankungen |
| ASXL1ASXL transcriptional regulator 1 | Häufig (30–79 %) | In 2 Erkrankungen |
| BMP6bone morphogenetic protein 6 | Häufig (30–79 %) | In 1 Erkrankung |
| C4Acomplement C4A (Chido/Rodgers blood group) | Häufig (30–79 %) | In 1 Erkrankung |
| CALRcalreticulin | Häufig (30–79 %) | In 1 Erkrankung |
| CBLCbl proto-oncogene | Häufig (30–79 %) | In 1 Erkrankung |
| CCR1C-C motif chemokine receptor 1 | Häufig (30–79 %) | In 1 Erkrankung |
| CD55CD55 molecule (Cromer blood group) | Häufig (30–79 %) | In 1 Erkrankung |
| CDKN1Bcyclin dependent kinase inhibitor 1B | Häufig (30–79 %) | In 1 Erkrankung |
| CDKN2Bcyclin dependent kinase inhibitor 2B | Häufig (30–79 %) | In 1 Erkrankung |
| CLCNKBchloride voltage-gated channel Kb | Häufig (30–79 %) | In 1 Erkrankung |
| CLDN16claudin 16 | Häufig (30–79 %) | In 1 Erkrankung |
| CLPBClpB family mitochondrial disaggregase | Häufig (30–79 %) | In 1 Erkrankung |
| CNBPCCHC-type zinc finger nucleic acid binding protein | Häufig (30–79 %) | In 1 Erkrankung |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Häufig (30–79 %) | In 1 Erkrankung |
| CTR9CTR9 component of Paf1/RNA polymerase II complex | Häufig (30–79 %) | In 1 Erkrankung |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Häufig (30–79 %) | In 1 Erkrankung |
| DNASE1L3deoxyribonuclease 1L3 | Häufig (30–79 %) | In 1 Erkrankung |
| ELANEelastase, neutrophil expressed | Häufig (30–79 %) | In 2 Erkrankungen |
| ELF4E74 like ETS transcription factor 4 | Häufig (30–79 %) | In 1 Erkrankung |
| EPORerythropoietin receptor | Häufig (30–79 %) | In 1 Erkrankung |
| ERAP1endoplasmic reticulum aminopeptidase 1 | Häufig (30–79 %) | In 1 Erkrankung |
| F5coagulation factor V | Häufig (30–79 %) | In 1 Erkrankung |
| FASFas cell surface death receptor | Häufig (30–79 %) | In 1 Erkrankung |
| GBA1glucosylceramidase beta 1 | Häufig (30–79 %) | In 1 Erkrankung |
| GCGRglucagon receptor | Häufig (30–79 %) | In 2 Erkrankungen |
| GFI1growth factor independent 1 transcriptional repressor | Häufig (30–79 %) | In 1 Erkrankung |
| GNA11G protein subunit alpha 11 | Häufig (30–79 %) | In 1 Erkrankung |
| GOSR2golgi SNAP receptor complex member 2 | Häufig (30–79 %) | In 1 Erkrankung |
| GPC3glypican 3 | Häufig (30–79 %) | In 1 Erkrankung |
| H19H19 imprinted maternally expressed transcript | Häufig (30–79 %) | In 1 Erkrankung |
| HFEhomeostatic iron regulator | Häufig (30–79 %) | In 2 Erkrankungen |
| HLA-Bmajor histocompatibility complex, class I, B | Häufig (30–79 %) | In 4 Erkrankungen |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | Häufig (30–79 %) | In 1 Erkrankung |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | Häufig (30–79 %) | In 1 Erkrankung |
| IFNGR1interferon gamma receptor 1 | Häufig (30–79 %) | In 1 Erkrankung |
| IL10interleukin 10 | Häufig (30–79 %) | In 1 Erkrankung |
| IL12Ainterleukin 12A | Häufig (30–79 %) | In 1 Erkrankung |
| IL12A-AS1IL12A antisense RNA 1 | Häufig (30–79 %) | In 1 Erkrankung |
| IL23Rinterleukin 23 receptor | Häufig (30–79 %) | In 1 Erkrankung |
| KLRC4killer cell lectin like receptor C4 | Häufig (30–79 %) | In 1 Erkrankung |
| MED12mediator complex subunit 12 | Häufig (30–79 %) | In 1 Erkrankung |
| MEN1menin 1 | Häufig (30–79 %) | In 1 Erkrankung |
| MITFmelanocyte inducing transcription factor | Häufig (30–79 %) | In 1 Erkrankung |
| NKX2-5NK2 homeobox 5 | Häufig (30–79 %) | In 1 Erkrankung |
| NLRP3NLR family pyrin domain containing 3 | Häufig (30–79 %) | In 2 Erkrankungen |
| NOD2nucleotide binding oligomerization domain containing 2 | Häufig (30–79 %) | In 2 Erkrankungen |
| OTULINOTU deubiquitinase with linear linkage specificity | Häufig (30–79 %) | In 1 Erkrankung |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Häufig (30–79 %) | In 1 Erkrankung |
| POU6F2POU class 6 homeobox 2 | Häufig (30–79 %) | In 1 Erkrankung |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Häufig (30–79 %) | In 2 Erkrankungen |
| PRTN3proteinase 3 | Häufig (30–79 %) | In 1 Erkrankung |
| PTENphosphatase and tensin homolog | Häufig (30–79 %) | In 1 Erkrankung |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Häufig (30–79 %) | In 2 Erkrankungen |
| RBCK1RANBP2-type and C3HC4-type zinc finger containing 1 | Häufig (30–79 %) | In 1 Erkrankung |
| RESTRE1 silencing transcription factor | Häufig (30–79 %) | In 1 Erkrankung |
| RIPK1receptor interacting serine/threonine kinase 1 | Häufig (30–79 %) | In 1 Erkrankung |
| RUNX1RUNX family transcription factor 1 | Häufig (30–79 %) | In 1 Erkrankung |
| SAA1serum amyloid A1 | Häufig (30–79 %) | In 1 Erkrankung |
| SCARB2scavenger receptor class B member 2 | Häufig (30–79 %) | In 1 Erkrankung |
| SCN1Bsodium voltage-gated channel beta subunit 1 | Häufig (30–79 %) | In 1 Erkrankung |
| SCN5Asodium voltage-gated channel alpha subunit 5 | Häufig (30–79 %) | In 1 Erkrankung |
| SDHDsuccinate dehydrogenase complex subunit D | Häufig (30–79 %) | In 1 Erkrankung |
| SLC12A3solute carrier family 12 member 3 | Häufig (30–79 %) | In 2 Erkrankungen |
| SRP19signal recognition particle 19 | Häufig (30–79 %) | In 1 Erkrankung |
| SRSF2serine and arginine rich splicing factor 2 | Häufig (30–79 %) | In 2 Erkrankungen |
| STAT4signal transducer and activator of transcription 4 | Häufig (30–79 %) | In 2 Erkrankungen |
| TCIRG1T cell immune regulator 1, ATPase H+ transporting V0 subunit a3 | Häufig (30–79 %) | In 1 Erkrankung |
| TERTtelomerase reverse transcriptase | Häufig (30–79 %) | In 1 Erkrankung |
| TET2tet methylcytosine dioxygenase 2 | Häufig (30–79 %) | In 2 Erkrankungen |
| TLR4toll like receptor 4 | Häufig (30–79 %) | In 1 Erkrankung |
| TRIM28tripartite motif containing 28 | Häufig (30–79 %) | In 1 Erkrankung |
| TRIP13thyroid hormone receptor interactor 13 | Häufig (30–79 %) | In 1 Erkrankung |
| TRPM4transient receptor potential cation channel subfamily M member 4 | Häufig (30–79 %) | In 1 Erkrankung |
| TSC1TSC complex subunit 1 | Häufig (30–79 %) | In 1 Erkrankung |
| TSC2TSC complex subunit 2 | Häufig (30–79 %) | In 1 Erkrankung |
| UBAC2UBA domain containing 2 | Häufig (30–79 %) | In 1 Erkrankung |
| UQCRHubiquinol-cytochrome c reductase hinge protein | Häufig (30–79 %) | In 1 Erkrankung |
| ZNRF3zinc and ring finger 3 | Häufig (30–79 %) | In 1 Erkrankung |
| ABCC2ATP binding cassette subfamily C member 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| ACTN4actinin alpha 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| ALDH4A1aldehyde dehydrogenase 4 family member A1 | Manchmal (5–29 %) | In 1 Erkrankung |
| ALG8ALG8 alpha-1,3-glucosyltransferase | Manchmal (5–29 %) | In 1 Erkrankung |
| ANK1ankyrin 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| ANKFY1ankyrin repeat and FYVE domain containing 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| ANLNanillin, actin binding protein | Manchmal (5–29 %) | In 1 Erkrankung |
| APOL1apolipoprotein L1 | Manchmal (5–29 %) | In 1 Erkrankung |
| ARHGAP24Rho GTPase activating protein 24 | Manchmal (5–29 %) | In 1 Erkrankung |
| ARHGDIARho GDP dissociation inhibitor alpha | Manchmal (5–29 %) | In 1 Erkrankung |
| ATP7BATPase copper transporting beta | Manchmal (5–29 %) | In 1 Erkrankung |
| AVILadvillin | Manchmal (5–29 %) | In 1 Erkrankung |
| BCL10BCL10 immune signaling adaptor | Manchmal (5–29 %) | In 1 Erkrankung |
| BCL11ABCL11 transcription factor A | Manchmal (5–29 %) | In 1 Erkrankung |
| BCORBCL6 corepressor | Manchmal (5–29 %) | In 1 Erkrankung |
| BIRC3baculoviral IAP repeat containing 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| BNC2basonuclin zinc finger protein 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| CCND1cyclin D1 | Manchmal (5–29 %) | In 1 Erkrankung |
| CD2APCD2 associated protein | Manchmal (5–29 %) | In 1 Erkrankung |
| CD46CD46 molecule | Manchmal (5–29 %) | In 1 Erkrankung |
| CFHcomplement factor H | Manchmal (5–29 %) | In 1 Erkrankung |
| CFIcomplement factor I | Manchmal (5–29 %) | In 1 Erkrankung |
| COL4A3collagen type IV alpha 3 chain | Manchmal (5–29 %) | In 1 Erkrankung |
| COQ8Bcoenzyme Q8B | Manchmal (5–29 %) | In 1 Erkrankung |
| CORINcorin, serine peptidase | Manchmal (5–29 %) | In 1 Erkrankung |
| CRB2crumbs cell polarity complex component 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| DAAM2dishevelled associated activator of morphogenesis 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| DDIT3DNA damage inducible transcript 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| DMPKDM1 protein kinase | Manchmal (5–29 %) | In 1 Erkrankung |
| EMP2epithelial membrane protein 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| EPB42erythrocyte membrane protein band 4.2 | Manchmal (5–29 %) | In 1 Erkrankung |
| FGF13fibroblast growth factor 13 | Manchmal (5–29 %) | In 1 Erkrankung |
| FIP1L1factor interacting with PAPOLA and CPSF1 | Manchmal (5–29 %) | In 1 Erkrankung |
| FLT1fms related receptor tyrosine kinase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| FOXP1forkhead box P1 | Manchmal (5–29 %) | In 1 Erkrankung |
| FUSFUS RNA binding protein | Manchmal (5–29 %) | In 1 Erkrankung |
| GAPVD1GTPase activating protein and VPS9 domains 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| GPR35G protein-coupled receptor 35 | Manchmal (5–29 %) | In 1 Erkrankung |
| HBBhemoglobin subunit beta | Manchmal (5–29 %) | In 3 Erkrankungen |
| HBG1hemoglobin subunit gamma 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| HBG2hemoglobin subunit gamma 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| HELLPARHELLP associated long non-coding RNA | Manchmal (5–29 %) | In 1 Erkrankung |
| HIVEP2HIVEP zinc finger 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Manchmal (5–29 %) | In 2 Erkrankungen |
| IGHimmunoglobulin heavy locus | Manchmal (5–29 %) | In 1 Erkrankung |
| IKZF1IKAROS family zinc finger 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| IL6interleukin 6 | Manchmal (5–29 %) | In 2 Erkrankungen |
| INF2inverted formin 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| IRAK1interleukin 1 receptor associated kinase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| IRF2BP2interferon regulatory factor 2 binding protein 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| KANK2KN motif and ankyrin repeat domains 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| KCNN4potassium calcium-activated channel subfamily N member 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| KITKIT proto-oncogene, receptor tyrosine kinase | Manchmal (5–29 %) | In 2 Erkrankungen |
| KLF1KLF transcription factor 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| LACC1laccase domain multifunctional purine nucleosidase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| LAMA5laminin subunit alpha 5 | Manchmal (5–29 %) | In 1 Erkrankung |
| LRP5LDL receptor related protein 5 | Manchmal (5–29 %) | In 1 Erkrankung |
| MAGI2membrane associated guanylate kinase, WW and PDZ domain containing 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| MALT1MALT1 paracaspase | Manchmal (5–29 %) | In 1 Erkrankung |
| MIFmacrophage migration inhibitory factor | Manchmal (5–29 %) | In 1 Erkrankung |
| MMUTmethylmalonyl-CoA mutase | Manchmal (5–29 %) | In 1 Erkrankung |
| MST1macrophage stimulating 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| MYCMYC proto-oncogene, bHLH transcription factor | Manchmal (5–29 %) | In 1 Erkrankung |
| MYO1Emyosin IE | Manchmal (5–29 %) | In 1 Erkrankung |
| NABP1nucleic acid binding protein 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| NPHS1NPHS1 adhesion molecule, nephrin | Manchmal (5–29 %) | In 1 Erkrankung |
| NPHS2NPHS2 stomatin family member, podocin | Manchmal (5–29 %) | In 1 Erkrankung |
| NPM1nucleophosmin 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| NUMA1nuclear mitotic apparatus protein 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| NUP107nucleoporin 107 | Manchmal (5–29 %) | In 1 Erkrankung |
| NUP133nucleoporin 133 | Manchmal (5–29 %) | In 1 Erkrankung |
| NUP160nucleoporin 160 | Manchmal (5–29 %) | In 1 Erkrankung |
| NUP205nucleoporin 205 | Manchmal (5–29 %) | In 1 Erkrankung |
| NUP37nucleoporin 37 | Manchmal (5–29 %) | In 1 Erkrankung |
| NUP85nucleoporin 85 | Manchmal (5–29 %) | In 1 Erkrankung |
| NUP93nucleoporin 93 | Manchmal (5–29 %) | In 1 Erkrankung |
| OTCornithine transcarbamylase | Manchmal (5–29 %) | In 1 Erkrankung |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| PAX2paired box 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Manchmal (5–29 %) | In 1 Erkrankung |
| PLCE1phospholipase C epsilon 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| PMLPML nuclear body scaffold | Manchmal (5–29 %) | In 1 Erkrankung |
| POMT1protein O-mannosyltransferase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| PORCNporcupine O-acyltransferase | Manchmal (5–29 %) | In 1 Erkrankung |
| PRKCSHPRKCSH beta subunit of glucosidase II | Manchmal (5–29 %) | In 1 Erkrankung |
| PTPN3protein tyrosine phosphatase non-receptor type 3 | Manchmal (5–29 %) | In 1 Erkrankung |
| PTPROprotein tyrosine phosphatase receptor type O | Manchmal (5–29 %) | In 1 Erkrankung |
| RARAretinoic acid receptor alpha | Manchmal (5–29 %) | In 1 Erkrankung |
| RNF168ring finger protein 168 | Manchmal (5–29 %) | In 1 Erkrankung |
| ROS1ROS proto-oncogene 1, receptor tyrosine kinase | Manchmal (5–29 %) | In 1 Erkrankung |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SEC63SEC63 protein translocation regulator | Manchmal (5–29 %) | In 1 Erkrankung |
| SEMA4Dsemaphorin 4D | Manchmal (5–29 %) | In 1 Erkrankung |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Manchmal (5–29 %) | In 2 Erkrankungen |
| SMPD1sphingomyelin phosphodiesterase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SPP1secreted phosphoprotein 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SPTA1spectrin alpha, erythrocytic 1 | Manchmal (5–29 %) | In 2 Erkrankungen |
| SPTBspectrin beta, erythrocytic | Manchmal (5–29 %) | In 2 Erkrankungen |
| STAT3signal transducer and activator of transcription 3 | Manchmal (5–29 %) | In 2 Erkrankungen |
| STAT5Bsignal transducer and activator of transcription 5B | Manchmal (5–29 %) | In 1 Erkrankung |
| STOX1storkhead box 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| SYKspleen associated tyrosine kinase | Manchmal (5–29 %) | In 1 Erkrankung |
| TBC1D8BTBC1 domain family member 8B | Manchmal (5–29 %) | In 1 Erkrankung |
| TBK1TANK binding kinase 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| TBL1XR1TBL1X/Y related 1 | Manchmal (5–29 %) | In 1 Erkrankung |
| TCF4transcription factor 4 | Manchmal (5–29 %) | In 1 Erkrankung |
| TFR2transferrin receptor 2 | Manchmal (5–29 %) | In 1 Erkrankung |
| TREHtrehalase | Manchmal (5–29 %) | In 2 Erkrankungen |
| TRPC6transient receptor potential cation channel subfamily C member 6 | Manchmal (5–29 %) | In 1 Erkrankung |
| UNC45Aunc-45 myosin chaperone A | Manchmal (5–29 %) | In 1 Erkrankung |
| VHLvon Hippel-Lindau tumor suppressor | Manchmal (5–29 %) | In 1 Erkrankung |
| ZBTB16zinc finger and BTB domain containing 16 | Manchmal (5–29 %) | In 1 Erkrankung |
| ABCB11ATP binding cassette subfamily B member 11 | Selten (1–4 %) | In 1 Erkrankung |
| ABCB4ATP binding cassette subfamily B member 4 | Selten (1–4 %) | In 1 Erkrankung |
| ATP8B1ATPase phospholipid transporting 8B1 | Selten (1–4 %) | In 1 Erkrankung |
| EPB41erythrocyte membrane protein band 4.1 | Selten (1–4 %) | In 1 Erkrankung |
| GYPCglycophorin C (Gerbich blood group) | Selten (1–4 %) | In 1 Erkrankung |
| NR1H4nuclear receptor subfamily 1 group H member 4 | Selten (1–4 %) | In 1 Erkrankung |
| SPTBN1spectrin beta, non-erythrocytic 1 | Selten (1–4 %) | In 1 Erkrankung |
| ABCG8ATP binding cassette subfamily G member 8 | Nicht erfasst | In 1 Erkrankung |
| ACTG2actin gamma 2, smooth muscle | Nicht erfasst | In 1 Erkrankung |
| ADA2adenosine deaminase 2 | Nicht erfasst | In 1 Erkrankung |
| BMP2bone morphogenetic protein 2 | Nicht erfasst | In 1 Erkrankung |
| CELcarboxyl ester lipase | Nicht erfasst | In 1 Erkrankung |
| CFTRCF transmembrane conductance regulator | Nicht erfasst | In 1 Erkrankung |
| GUCY2Cguanylate cyclase 2C | Nicht erfasst | In 1 Erkrankung |
| HLA-DQA1major histocompatibility complex, class II, DQ alpha 1 | Nicht erfasst | In 1 Erkrankung |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Nicht erfasst | In 1 Erkrankung |
| HPS1HPS1 biogenesis of lysosomal organelles complex 3 subunit 1 | Nicht erfasst | In 1 Erkrankung |
| HS3ST6heparan sulfate-glucosamine 3-sulfotransferase 6 | Nicht erfasst | In 1 Erkrankung |
| KIF1Bkinesin family member 1B | Nicht erfasst | In 1 Erkrankung |
| MCM6minichromosome maintenance complex component 6 | Nicht erfasst | In 1 Erkrankung |
| MLYCDmalonyl-CoA decarboxylase | Nicht erfasst | In 1 Erkrankung |
| NLRP12NLR family pyrin domain containing 12 | Nicht erfasst | In 1 Erkrankung |
| OPLAH5-oxoprolinase, ATP-hydrolysing | Nicht erfasst | In 1 Erkrankung |
| SLC25A26solute carrier family 25 member 26 | Nicht erfasst | In 1 Erkrankung |
| SPINK1serine peptidase inhibitor Kazal type 1 | Nicht erfasst | In 2 Erkrankungen |
Wie häufig dieses Merkmal bei Menschen mit einer der Erkrankungen auftritt, die mit dem Gen in Verbindung stehen, und zwar der höchste Wert unter ihnen, so wie ihn die Human Phenotype Ontology erfasst. Diese Seiten beschreiben Merkmale und die dazugehörige Forschung; sie stellen keine Diagnose dar. Fragen zu Symptomen richten Sie bitte an Ihre Ärztin, Ihren Arzt oder eine genetische Beratung.
Untergeordnete Merkmale
Übergeordnete Merkmale
Woher diese Angaben stammen
- Die Human Phenotype Ontology, Version 2026-09-01: das Merkmal, seine Bezeichnungen, seine Definition und die damit verknüpften Gene. Weitere Informationen finden Sie unter hpo.jax.org.
- Datenstand 2026.10.19-9814e911.
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