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Træk
Hypospadias
Abnormal position of urethral meatus on the ventral penile shaft (underside) characterized by displacement of the urethral meatus from the tip of the glans penis to the ventral surface of the penis, scrotum, or perineum.
Resumé
- Også kaldet
- Hypospadia
- Kropssystem
- Abnormality of the genitourinary system
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Denne side som data
Tilføj .json til sidens adresse, eller bed om application/json, for at læse den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/hypospadias.json"
page <- fromJSON(url)
page$trait$nameHypospadiasHP:0000047
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Log indSpørgSekvenér dit genom↗
Læs de gener, der er knyttet til Hypospadias, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test159 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.
- Fanconi AnemiaReads 18 of these genesBRCA1BRCA2BRIP1ERCC4FANCAFANCBAbout this report →
- Diamond-Blackfan AnemiaReads 14 of these genesGATA1HEATR3RPL11RPL15RPL26RPL35AAbout this report →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 13 of these genesPEX1PEX10PEX11BPEX12PEX13PEX14About this report →
- Coffin-Siris SyndromeReads 12 of these genesARID1AARID1BARID2BICRADPF2SMARCA4About this report →
Show 155 more reports
- DNA Repair DiseaseReads 18 of these genesBRCA1BRCA2BRIP1ERCC4FANCAFANCBAbout this report →
- Intellectual DisabilityReads 41 of these genesZMYM3MECP2NSD2PIGGATP6AP2BRD4About this report →
- Cornelia de Lange SyndromeReads 6 of these genesBRD4HDAC8NIPBLRAD21SMC1ASMC3About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 10 of these genesDHX37GATA4HSD17B3MAP3K1NR5A1SRYAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 6 of these genesCDKN1CHMGA2IGF2PLAG1H19NSD1About this report →
- Congenital Adrenal HyperplasiaReads 5 of these genesCYP17A1HSD3B2PORCYP21A2STARAbout this report →
- Other Inherited LeukodystrophiesReads 16 of these genesPEX1PEX10PEX11BPEX12PEX13PEX14About this report →
- Hypertrophic CardiomyopathyReads 14 of these genesCDKN1CDHX37MAP3K1NR5A1SRYZFPM2About this report →
- Fraser SyndromeReads 3 of these genesFRAS1FREM2GRIP1About this report →
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 3 of these genesSMARCA4SMARCB1SMARCE1About this report →
- 46,XX Differences of Sex DevelopmentReads 3 of these genesNR5A1SRYRSPO1About this report →
- Syndromic CraniosynostosisReads 7 of these genesFGFR2RNU12PORSKITCF12FGFR1About 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 →
- Kabuki SyndromeReads 2 of these genesKDM6AKMT2DAbout this report →
- Müllerian Aplasia (MRKH Syndrome)Reads 2 of these genesWNT4TBX6About this report →
- Rare Hereditary Peripheral NeuropathiesReads 21 of these genesNDUFS4PRPS1FIG4PEX1PEX10PEX11BAbout this report →
- Inherited Neurodegenerative DisordersReads 26 of these genesLETM1WWOXARFIG4PEX1PEX10About this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 3 of these genesCYB5AHBA1HBA2About this report →
- Congenital Disorders of GlycosylationReads 13 of these genesPIGGATP6AP2B3GLCTCOG1ALG12DLL3About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 6 of these genesBCORCOX7BHCCSMAB21L2NDUFB11SOX2About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 3 of these genesEVCEVC2WDR35About this report →
- Congenital MyopathiesReads 5 of these genesACTA1KLHL40KLHL41LMOD3NEBAbout this report →
- Noonan SyndromeReads 5 of these genesBRAFKRASMAP2K1PTPN11RAF1About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 3 of these genesPAX6FOXC1PITX2About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 3 of these genesBRIP1PALB2RAD51CAbout this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 2 of these genesRERESOX11About this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- Aarskog-Scott SyndromeReads 1 of these genesFGD1About this report →
- Alveolar Capillary Dysplasia with Misalignment of Pulmonary VeinsReads 1 of these genesFOXF1About this report →
- Alzahrani-Kuwahara SyndromeReads 1 of these genesSMG8About this report →
- Androgen Insensitivity SyndromeReads 1 of these genesARAbout this report →
- Beaulieu-Boycott-Innes Syndrome (THOC6)Reads 1 of these genesTHOC6About this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- Campomelic DysplasiaReads 1 of these genesSOX9About this report →
- CHRNG-Related Multiple Pterygium SyndromeReads 1 of these genesCHRNGAbout this report →
- Craniofrontonasal SyndromeReads 1 of these genesEFNB1About this report →
- DCMA Syndrome (3-Methylglutaconic Aciduria Type 5)Reads 1 of these genesDNAJC19About this report →
- Deficiency of Adenosine Deaminase 2 (DADA2)Reads 1 of these genesADA2About this report →
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- Elsahy-Waters SyndromeReads 1 of these genesCDH11About this report →
- FANCM-Related Genomic Instability DisorderReads 1 of these genesFANCMAbout this report →
- FAT4-Related Neurodevelopmental DisorderReads 1 of these genesFAT4About this report →
- Floating-Harbor SyndromeReads 1 of these genesSRCAPAbout this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- Hajdu-Cheney SyndromeReads 1 of these genesNOTCH2About this report →
- Hand-Foot-Genital SyndromeReads 1 of these genesHOXA13About this report →
- IFAP Syndrome (MBTPS2)Reads 1 of these genesMBTPS2About this report →
- Johanson-Blizzard SyndromeReads 1 of these genesUBR1About this report →
- KAT6B-Related DisordersReads 1 of these genesKAT6BAbout this report →
- KDM1A-Related Neurodevelopmental DisorderReads 1 of these genesKDM1AAbout this report →
- Meier-Gorlin Syndrome 3 (ORC6)Reads 1 of these genesORC6About this report →
- Meier-Gorlin Syndrome 4Reads 1 of these genesCDT1About this report →
- Meier-Gorlin Syndrome 7 (CDC45)Reads 1 of these genesCDC45About this report →
- Microcephalic Osteodysplastic Primordial Dwarfism Type IIReads 1 of these genesPCNTAbout this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- Nizon-Isidor SyndromeReads 1 of these genesMED12LAbout this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- Perlman SyndromeReads 1 of these genesDIS3L2About this report →
- POLR3A-Related DisorderReads 1 of these genesPOLR3AAbout this report →
- Radio-Tartaglia SyndromeReads 1 of these genesSPENAbout this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- Roberts SyndromeReads 1 of these genesESCO2About this report →
- RTTN-Related Microcephalic Primordial DwarfismReads 1 of these genesRTTNAbout this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- Short-Rib Thoracic Dysplasia 7 (WDR35)Reads 1 of these genesWDR35About this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- Spinal and Bulbar Muscular Atrophy (Kennedy Disease)Reads 1 of these genesARAbout this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
- Stankiewicz-Isidor SyndromeReads 1 of these genesPSMD12About this report →
- TMEM94-Related Intellectual Disability with Heart DefectsReads 1 of these genesTMEM94About this report →
- Townes-Brocks SyndromeReads 1 of these genesSALL1About this report →
- TRIM8-Related Neurodevelopmental and Kidney DisorderReads 1 of these genesTRIM8About this report →
- X-Linked Opitz G/BBB SyndromeReads 1 of these genesMID1About this report →
- Mosaic Variegated Aneuploidy SyndromeReads 2 of these genesTRIP13BUB1BAbout this report →
- ThalassaemiaReads 2 of these genesHBA1HBA2About this report →
- Female InfertilityReads 6 of these genesNR5A1TP63WNT4FANCMTRIP13STARAbout this report →
- Epilepsy (Full Panel)Reads 11 of these genesCPLX1MECP2WWOXATP6AP2FLNAPUM1About this report →
- Primary Mitochondrial DiseaseReads 9 of these genesNDUFA8NDUFS4TMEM70FBXL4GFM1LRPPRCAbout this report →
- PolycythemiaReads 2 of these genesHBA1HBA2About this report →
- Alagille SyndromeReads 1 of these genesNOTCH2About this report →
- Hereditary Gingival FibromatosisReads 1 of these genesRESTAbout this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- GPI Anchor Biosynthesis DefectsReads 3 of these genesPIGGPIGAPIGNAbout this report →
- Kidney CancerReads 2 of these genesPAX6TRIM28About this report →
- Joubert Syndrome And Related DisordersReads 4 of these genesB9D2KIF7CSPP1KIAA0586About this report →
- Bardet-Biedl and Alström SyndromesReads 3 of these genesBBS2MKKSTTC8About this report →
- Lissencephaly Spectrum DisordersReads 3 of these genesARXPSPHAPC2About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 3 of these genesZFXZMYM2SETD5About this report →
- Leigh SyndromeReads 5 of these genesNDUFS4FBXL4GFM1LRPPRCSUCLG1About this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Urinary and Renal System TumourReads 2 of these genesPAX6TRIM28About this report →
- Congenital Diaphragmatic Hernia (Monogenic)Reads 1 of these genesZFPM2About this report →
- EBV-Driven Lymphoproliferation and CARD11 Immune DysregulationReads 1 of these genesIKZF2About this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesKIFBPAbout this report →
- Tetralogy of FallotReads 1 of these genesZFPM2About this report →
- Hypogonadotropic HypogonadismReads 4 of these genesNR0B1SMCHD1TCF12FGFR1About this report →
- Inherited Congenital Heart DefectsReads 2 of these genesGATA4FLNAAbout this report →
- Diabetes MellitusReads 3 of these genesGATA4PAX6HNF1BAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 4 of these genesWWOXPEX6CSPP1KIAA0586About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 2 of these genesTUBBAPC2About this report →
- Inherited ThrombocytopeniasReads 3 of these genesCDC42GATA1GP1BBAbout this report →
- Congenital Dyserythropoietic AnaemiasReads 1 of these genesKLF1About this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Inherited Predisposition to Myeloid Blood CancersReads 1 of these genesSAMD9About this report →
- NeurofibromatosisReads 1 of these genesSMARCB1About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesPDE4DAbout this report →
- TubulinopathiesReads 1 of these genesTUBBAbout this report →
- Neonatal Diabetes MellitusReads 2 of these genesGATA4HNF1BAbout this report →
- Autosomal Dominant Tubulointerstitial Kidney DiseaseReads 1 of these genesHNF1BAbout this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesMTORAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Autoimmune DiseaseReads 2 of these genesKRASCHRNGAbout this report →
- Dilated CardiomyopathyReads 3 of these genesLMNAPRDM16RAF1About this report →
- Dyskeratosis CongenitaReads 2 of these genesCDCA7DKC1About this report →
- Hereditary Orofacial CleftingReads 1 of these genesTBX22About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 2 of these genesTMEM63APOLR3AAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Colorectal Cancer & PolyposisReads 1 of these genesPOLEAbout this report →
- Disorders of Glycine & Serine MetabolismReads 1 of these genesPSPHAbout this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR0B1About this report →
- GlaucomaReads 1 of these genesFOXC1About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Purine & Pyrimidine Metabolism DisordersReads 1 of these genesPRPS1About this report →
- Osteogenesis ImperfectaReads 2 of these genesMBTPS2POLR3AAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 2 of these genesADA2SKIC3About this report →
- Other Inborn Errors of ImmunityReads 5 of these genesIKZF2DPP9KRASSKIC3TBX1About this report →
- Charcot-Marie-Tooth DiseaseReads 3 of these genesPRPS1FIG4LMNAAbout this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 2 of these genesMBTPS2RSPO1About this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BBAbout this report →
- Hereditary Pheochromocytoma and ParagangliomaReads 1 of these genesMAXAbout this report →
- Marfan Like SyndromesReads 1 of these genesSKIAbout this report →
- Meckel SyndromeReads 1 of these genesB9D2About this report →
- Maturity-Onset Diabetes Of The YoungReads 1 of these genesHNF1BAbout this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 1 of these genesLSSAbout this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 1 of these genesFAT4About this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesCEP152About this report →
- Ectodermal DysplasiasReads 1 of these genesTP63About this report →
- Retinitis PigmentosaReads 2 of these genesBBS2TTC8About this report →
- Congenital HypothyroidismReads 1 of these genesNKX2-1About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesCOL3A1About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesLSSAbout this report →
- Hearing Loss and DeafnessReads 2 of these genesIKZF2PRPS1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesGLI3About this report →
- Spinal Muscular AtrophyReads 1 of these genesUBA1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesFIG4About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesPUM1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesVAC14About this report →
- Male InfertilityReads 1 of these genesFANCMAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesWASHC5About this report →
Læs de gener, der er knyttet til Hypospadias, og resten af dit genom, med én test.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger
Bestil min Genome Test384 gener knyttet til Hypospadias
Ændringer i disse gener forårsager sjældne tilstande, hvor Hypospadias ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| B9D2B9 domain containing 2 | Altid | I 1 tilstand |
| CACHD1cache domain containing 1 | Altid | I 1 tilstand |
| CDH11cadherin 11 | Altid | I 2 tilstande |
| DHRS3dehydrogenase/reductase 3 | Altid | I 1 tilstand |
| FGFR2fibroblast growth factor receptor 2 | Altid | I 1 tilstand |
| FRYLFRY like transcription coactivator | Altid | I 1 tilstand |
| H4C11H4 clustered histone 11 | Altid | I 1 tilstand |
| IKZF2IKAROS family zinc finger 2 | Altid | I 1 tilstand |
| JKAMPJNK1/MAPK8 associated membrane protein | Altid | I 1 tilstand |
| KLF1KLF transcription factor 1 | Altid | I 2 tilstande |
| MAN2B2mannosidase alpha class 2B member 2 | Altid | I 1 tilstand |
| MED25mediator complex subunit 25 | Altid | I 2 tilstande |
| MSL2MSL complex subunit 2 | Altid | I 1 tilstand |
| NDUFA8NADH:ubiquinone oxidoreductase subunit A8 | Altid | I 1 tilstand |
| NDUFB7NADH:ubiquinone oxidoreductase subunit B7 | Altid | I 1 tilstand |
| NDUFS4NADH:ubiquinone oxidoreductase subunit S4 | Altid | I 1 tilstand |
| PPP1R12Aprotein phosphatase 1 regulatory subunit 12A | Altid | I 1 tilstand |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Altid | I 1 tilstand |
| PTBP1polypyrimidine tract binding protein 1 | Altid | I 1 tilstand |
| RNU12RNA, U12 small nuclear | Altid | I 2 tilstande |
| RNU5B-1RNA, U5B small nuclear 1 | Altid | I 1 tilstand |
| SAMD9sterile alpha motif domain containing 9 | Altid | I 1 tilstand |
| SLC25A10solute carrier family 25 member 10 | Altid | I 1 tilstand |
| SOX9SRY-box transcription factor 9 | Altid | I 4 tilstande |
| TOP2BDNA topoisomerase II beta | Altid | I 1 tilstand |
| ZMYM3zinc finger MYM-type containing 3 | Altid | I 1 tilstand |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Meget ofte (80–99 %) | I 3 tilstande |
| CPLX1complexin 1 | Meget ofte (80–99 %) | I 2 tilstande |
| CTBP1C-terminal binding protein 1 | Meget ofte (80–99 %) | I 2 tilstande |
| CUL7cullin 7 | Meget ofte (80–99 %) | I 2 tilstande |
| CYB5Acytochrome b5 type A | Meget ofte (80–99 %) | I 2 tilstande |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Meget ofte (80–99 %) | I 2 tilstande |
| DHX37DEAH-box helicase 37 | Meget ofte (80–99 %) | I 1 tilstand |
| GATA4GATA binding protein 4 | Meget ofte (80–99 %) | I 2 tilstande |
| HSD17B3hydroxysteroid 17-beta dehydrogenase 3 | Meget ofte (80–99 %) | I 1 tilstand |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Meget ofte (80–99 %) | I 2 tilstande |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Meget ofte (80–99 %) | I 2 tilstande |
| MECP2methyl-CpG binding protein 2 | Meget ofte (80–99 %) | I 2 tilstande |
| MID1midline 1 | Meget ofte (80–99 %) | I 2 tilstande |
| NELFAnegative elongation factor complex member A | Meget ofte (80–99 %) | I 1 tilstand |
Vis 344 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| NR0B1nuclear receptor subfamily 0 group B member 1 | Meget ofte (80–99 %) | I 1 tilstand |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Meget ofte (80–99 %) | I 2 tilstande |
| NSD2nuclear receptor binding SET domain protein 2 | Meget ofte (80–99 %) | I 2 tilstande |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Meget ofte (80–99 %) | I 1 tilstand |
| POLEDNA polymerase epsilon, catalytic subunit | Meget ofte (80–99 %) | I 2 tilstande |
| SRYsex determining region Y | Meget ofte (80–99 %) | I 4 tilstande |
| TBX22T-box transcription factor 22 | Meget ofte (80–99 %) | I 2 tilstande |
| TSHZ3teashirt zinc finger homeobox 3 | Meget ofte (80–99 %) | I 1 tilstand |
| VAMP7vesicle associated membrane protein 7 | Meget ofte (80–99 %) | I 1 tilstand |
| WT1WT1 transcription factor | Meget ofte (80–99 %) | I 3 tilstande |
| WWOXWW domain containing oxidoreductase | Meget ofte (80–99 %) | I 1 tilstand |
| ZFPM2zinc finger protein, FOG family member 2 | Meget ofte (80–99 %) | I 1 tilstand |
| ABL1ABL proto-oncogene 1, non-receptor tyrosine kinase | Ofte (30–79 %) | I 1 tilstand |
| ARandrogen receptor | Ofte (30–79 %) | I 1 tilstand |
| ATP6AP2ATPase H+ transporting accessory protein 2 | Ofte (30–79 %) | I 1 tilstand |
| B3GLCTbeta 3-glucosyltransferase | Ofte (30–79 %) | I 2 tilstande |
| BBS2Bardet-Biedl syndrome 2 | Ofte (30–79 %) | I 1 tilstand |
| BCORBCL6 corepressor | Ofte (30–79 %) | I 3 tilstande |
| BRD4bromodomain containing 4 | Ofte (30–79 %) | I 1 tilstand |
| CHRNA3cholinergic receptor nicotinic alpha 3 subunit | Ofte (30–79 %) | I 1 tilstand |
| COG1component of oligomeric golgi complex 1 | Ofte (30–79 %) | I 1 tilstand |
| CREBBPCREB binding lysine acetyltransferase | Ofte (30–79 %) | I 3 tilstande |
| DACT1dishevelled binding antagonist of beta catenin 1 | Ofte (30–79 %) | I 2 tilstande |
| DHCR77-dehydrocholesterol reductase | Ofte (30–79 %) | I 2 tilstande |
| DNAJC19DnaJ heat shock protein family (Hsp40) member C19 | Ofte (30–79 %) | I 1 tilstand |
| DOT1LDOT1 like histone lysine methyltransferase | Ofte (30–79 %) | I 1 tilstand |
| DVL1dishevelled segment polarity protein 1 | Ofte (30–79 %) | I 2 tilstande |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Ofte (30–79 %) | I 1 tilstand |
| EP300EP300 lysine acetyltransferase | Ofte (30–79 %) | I 2 tilstande |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Ofte (30–79 %) | I 2 tilstande |
| EVCEvC ciliary complex subunit 1 | Ofte (30–79 %) | I 2 tilstande |
| EVC2EvC ciliary complex subunit 2 | Ofte (30–79 %) | I 2 tilstande |
| FDFT1farnesyl-diphosphate farnesyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| FGFRL1fibroblast growth factor receptor like 1 | Ofte (30–79 %) | I 1 tilstand |
| FIG4FIG4 phosphoinositide 5-phosphatase | Ofte (30–79 %) | I 2 tilstande |
| FLNAfilamin A | Ofte (30–79 %) | I 2 tilstande |
| GINS3GINS complex subunit 3 | Ofte (30–79 %) | I 1 tilstand |
| GLI1GLI family zinc finger 1 | Ofte (30–79 %) | I 1 tilstand |
| HDAC8histone deacetylase 8 | Ofte (30–79 %) | I 1 tilstand |
| HMGA2high mobility group AT-hook 2 | Ofte (30–79 %) | I 1 tilstand |
| HNRNPH1heterogeneous nuclear ribonucleoprotein H1 | Ofte (30–79 %) | I 1 tilstand |
| HOXA13homeobox A13 | Ofte (30–79 %) | I 2 tilstande |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Ofte (30–79 %) | I 2 tilstande |
| IGF2insulin like growth factor 2 | Ofte (30–79 %) | I 2 tilstande |
| KAT5lysine acetyltransferase 5 | Ofte (30–79 %) | I 1 tilstand |
| KAT6Blysine acetyltransferase 6B | Ofte (30–79 %) | I 1 tilstand |
| KDM5Blysine demethylase 5B | Ofte (30–79 %) | I 1 tilstand |
| KIF7kinesin family member 7 | Ofte (30–79 %) | I 2 tilstande |
| LSM7LSM7 homolog, U6 small nuclear RNA and mRNA degradation associated | Ofte (30–79 %) | I 1 tilstand |
| LSSlanosterol synthase | Ofte (30–79 %) | I 1 tilstand |
| MAB21L1mab-21 like 1 | Ofte (30–79 %) | I 1 tilstand |
| MAU2MAU2 sister chromatid cohesion factor | Ofte (30–79 %) | I 1 tilstand |
| MAXMYC associated transcriptional regulator X | Ofte (30–79 %) | I 1 tilstand |
| MCTP2multiple C2 and transmembrane domain containing 2 | Ofte (30–79 %) | I 1 tilstand |
| MED12mediator complex subunit 12 | Ofte (30–79 %) | I 1 tilstand |
| MKKSMKKS centrosomal shuttling protein | Ofte (30–79 %) | I 1 tilstand |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Ofte (30–79 %) | I 2 tilstande |
| NIPBLNIPBL cohesin loading factor | Ofte (30–79 %) | I 2 tilstande |
| OGTO-linked N-acetylglucosamine (GlcNAc) transferase | Ofte (30–79 %) | I 1 tilstand |
| OTUD5OTU deubiquitinase 5 | Ofte (30–79 %) | I 1 tilstand |
| PAX6paired box 6 | Ofte (30–79 %) | I 1 tilstand |
| PEX1peroxisomal biogenesis factor 1 | Ofte (30–79 %) | I 2 tilstande |
| PEX10peroxisomal biogenesis factor 10 | Ofte (30–79 %) | I 1 tilstand |
| PEX11Bperoxisomal biogenesis factor 11 beta | Ofte (30–79 %) | I 1 tilstand |
| PEX12peroxisomal biogenesis factor 12 | Ofte (30–79 %) | I 1 tilstand |
| PEX13peroxisomal biogenesis factor 13 | Ofte (30–79 %) | I 1 tilstand |
| PEX14peroxisomal biogenesis factor 14 | Ofte (30–79 %) | I 1 tilstand |
| PEX16peroxisomal biogenesis factor 16 | Ofte (30–79 %) | I 1 tilstand |
| PEX19peroxisomal biogenesis factor 19 | Ofte (30–79 %) | I 1 tilstand |
| PEX2peroxisomal biogenesis factor 2 | Ofte (30–79 %) | I 2 tilstande |
| PEX26peroxisomal biogenesis factor 26 | Ofte (30–79 %) | I 1 tilstand |
| PEX3peroxisomal biogenesis factor 3 | Ofte (30–79 %) | I 1 tilstand |
| PEX5peroxisomal biogenesis factor 5 | Ofte (30–79 %) | I 1 tilstand |
| PEX6peroxisomal biogenesis factor 6 | Ofte (30–79 %) | I 1 tilstand |
| PLAG1PLAG1 zinc finger | Ofte (30–79 %) | I 1 tilstand |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Ofte (30–79 %) | I 1 tilstand |
| PTDSS1phosphatidylserine synthase 1 | Ofte (30–79 %) | I 2 tilstande |
| PUM1pumilio RNA binding family member 1 | Ofte (30–79 %) | I 1 tilstand |
| RAC1Rac family small GTPase 1 | Ofte (30–79 %) | I 2 tilstande |
| RAD21RAD21 cohesin complex component | Ofte (30–79 %) | I 1 tilstand |
| RPL10ribosomal protein L10 | Ofte (30–79 %) | I 3 tilstande |
| SIAH1siah E3 ubiquitin protein ligase 1 | Ofte (30–79 %) | I 1 tilstand |
| SMC1Astructural maintenance of chromosomes 1A | Ofte (30–79 %) | I 1 tilstand |
| SMC3structural maintenance of chromosomes 3 | Ofte (30–79 %) | I 1 tilstand |
| SMG8SMG8 nonsense mediated mRNA decay factor | Ofte (30–79 %) | I 1 tilstand |
| TMEM63Atransmembrane protein 63A | Ofte (30–79 %) | I 1 tilstand |
| TMEM70transmembrane protein 70 | Ofte (30–79 %) | I 2 tilstande |
| TP63tumor protein p63 | Ofte (30–79 %) | I 3 tilstande |
| TRIM8tripartite motif containing 8 | Ofte (30–79 %) | I 1 tilstand |
| VAC14VAC14 component of PIKFYVE complex | Ofte (30–79 %) | I 1 tilstand |
| WBP4WW domain binding protein 4 | Ofte (30–79 %) | I 1 tilstand |
| WNT4Wnt family member 4 | Ofte (30–79 %) | I 2 tilstande |
| ZEB2zinc finger E-box binding homeobox 2 | Ofte (30–79 %) | I 3 tilstande |
| ZFXzinc finger protein X-linked | Ofte (30–79 %) | I 1 tilstand |
| ACTA1actin alpha 1, skeletal muscle | Nogle gange (5–29 %) | I 1 tilstand |
| ADA2adenosine deaminase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ADAT3adenosine deaminase tRNA specific 3 | Nogle gange (5–29 %) | I 1 tilstand |
| AFF4ALF transcription elongation factor 4 | Nogle gange (5–29 %) | I 1 tilstand |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Nogle gange (5–29 %) | I 2 tilstande |
| ARID1AAT-rich interaction domain 1A | Nogle gange (5–29 %) | I 1 tilstand |
| ARID1BAT-rich interaction domain 1B | Nogle gange (5–29 %) | I 2 tilstande |
| ARID2AT-rich interaction domain 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ARVCFARVCF delta catenin family member | Nogle gange (5–29 %) | I 1 tilstand |
| ARXaristaless related homeobox | Nogle gange (5–29 %) | I 2 tilstande |
| BICRABRD4 interacting chromatin remodeling complex associated protein | Nogle gange (5–29 %) | I 1 tilstand |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Nogle gange (5–29 %) | I 2 tilstande |
| BRCA1BRCA1 DNA repair associated | Nogle gange (5–29 %) | I 1 tilstand |
| BRCA2BRCA2 DNA repair associated | Nogle gange (5–29 %) | I 2 tilstande |
| BRIP1BRCA1 interacting DNA helicase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CASZ1castor zinc finger 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CCDC22CCC complex scaffolding subunit CCDC22 | Nogle gange (5–29 %) | I 1 tilstand |
| CCDC8coiled-coil domain containing 8 subunit of 3M complex | Nogle gange (5–29 %) | I 1 tilstand |
| CDC42cell division cycle 42 | Nogle gange (5–29 %) | I 2 tilstande |
| CDC42BPBCDC42 binding protein kinase beta | Nogle gange (5–29 %) | I 1 tilstand |
| CDC45cell division cycle 45 | Nogle gange (5–29 %) | I 2 tilstande |
| CDC6cell division cycle 6 | Nogle gange (5–29 %) | I 1 tilstand |
| CDT1chromatin licensing and DNA replication factor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CEP152centrosomal protein 152 | Nogle gange (5–29 %) | I 1 tilstand |
| CILK1ciliogenesis associated kinase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| COL3A1collagen type III alpha 1 chain | Nogle gange (5–29 %) | I 1 tilstand |
| COLEC11collectin subfamily member 11 | Nogle gange (5–29 %) | I 1 tilstand |
| COMTcatechol-O-methyltransferase | Nogle gange (5–29 %) | I 1 tilstand |
| COX7Bcytochrome c oxidase subunit 7B | Nogle gange (5–29 %) | I 2 tilstande |
| CSPP1centrosome and spindle pole associated protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CTR9CTR9 component of Paf1/RNA polymerase II complex | Nogle gange (5–29 %) | I 1 tilstand |
| CUX1cut like homeobox 1 | Nogle gange (5–29 %) | I 1 tilstand |
| DCHS1dachsous cadherin-related 1 | Nogle gange (5–29 %) | I 2 tilstande |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Nogle gange (5–29 %) | I 1 tilstand |
| DLL3delta like canonical Notch ligand 3 | Nogle gange (5–29 %) | I 1 tilstand |
| DPF2double PHD fingers 2 | Nogle gange (5–29 %) | I 1 tilstand |
| DPP9dipeptidyl peptidase 9 | Nogle gange (5–29 %) | I 1 tilstand |
| DPYSL5dihydropyrimidinase like 5 | Nogle gange (5–29 %) | I 1 tilstand |
| DVL3dishevelled segment polarity protein 3 | Nogle gange (5–29 %) | I 1 tilstand |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Nogle gange (5–29 %) | I 2 tilstande |
| EFNB1ephrin B1 | Nogle gange (5–29 %) | I 2 tilstande |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Nogle gange (5–29 %) | I 1 tilstand |
| ERMARDER membrane associated RNA degradation | Nogle gange (5–29 %) | I 1 tilstand |
| FAAP100FA core complex associated protein 100 | Nogle gange (5–29 %) | I 1 tilstand |
| FANCAFA complementation group A | Nogle gange (5–29 %) | I 1 tilstand |
| FANCBFA complementation group B | Nogle gange (5–29 %) | I 1 tilstand |
| FANCCFA complementation group C | Nogle gange (5–29 %) | I 1 tilstand |
| FANCD2FA complementation group D2 | Nogle gange (5–29 %) | I 1 tilstand |
| FANCEFA complementation group E | Nogle gange (5–29 %) | I 1 tilstand |
| FANCFFA complementation group F | Nogle gange (5–29 %) | I 1 tilstand |
| FANCGFA complementation group G | Nogle gange (5–29 %) | I 1 tilstand |
| FANCIFA complementation group I | Nogle gange (5–29 %) | I 1 tilstand |
| FANCLFA complementation group L | Nogle gange (5–29 %) | I 1 tilstand |
| FANCMFA complementation group M | Nogle gange (5–29 %) | I 1 tilstand |
| FAT4FAT atypical cadherin 4 | Nogle gange (5–29 %) | I 2 tilstande |
| FBXL4F-box and leucine rich repeat protein 4 | Nogle gange (5–29 %) | I 1 tilstand |
| FGD1FYVE, RhoGEF and PH domain containing 1 | Nogle gange (5–29 %) | I 1 tilstand |
| FOCADfocadhesin | Nogle gange (5–29 %) | I 1 tilstand |
| FOXC1forkhead box C1 | Nogle gange (5–29 %) | I 1 tilstand |
| FOXF1forkhead box F1 | Nogle gange (5–29 %) | I 1 tilstand |
| FRAS1Fraser extracellular matrix complex subunit 1 | Nogle gange (5–29 %) | I 2 tilstande |
| FREM2FRAS1 related extracellular matrix 2 | Nogle gange (5–29 %) | I 1 tilstand |
| FZD2frizzled class receptor 2 | Nogle gange (5–29 %) | I 2 tilstande |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Nogle gange (5–29 %) | I 1 tilstand |
| GATA1GATA binding protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GATAD2BGATA zinc finger domain containing 2B | Nogle gange (5–29 %) | I 1 tilstand |
| GFM1G elongation factor mitochondrial 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GLI3GLI family zinc finger 3 | Nogle gange (5–29 %) | I 4 tilstande |
| GMNNgeminin DNA replication inhibitor | Nogle gange (5–29 %) | I 1 tilstand |
| GP1BBglycoprotein Ib platelet subunit beta | Nogle gange (5–29 %) | I 1 tilstand |
| GPC3glypican 3 | Nogle gange (5–29 %) | I 3 tilstande |
| GPC4glypican 4 | Nogle gange (5–29 %) | I 1 tilstand |
| GRB10growth factor receptor bound protein 10 | Nogle gange (5–29 %) | I 1 tilstand |
| GRIP1glutamate receptor interacting protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| H19H19 imprinted maternally expressed transcript | Nogle gange (5–29 %) | I 1 tilstand |
| HBA1hemoglobin subunit alpha 1 | Nogle gange (5–29 %) | I 1 tilstand |
| HBA2hemoglobin subunit alpha 2 | Nogle gange (5–29 %) | I 1 tilstand |
| HCCSholocytochrome c synthase | Nogle gange (5–29 %) | I 2 tilstande |
| HEATR3HEAT repeat containing 3 | Nogle gange (5–29 %) | I 1 tilstand |
| HES7hes family bHLH transcription factor 7 | Nogle gange (5–29 %) | I 1 tilstand |
| HIRAhistone cell cycle regulator | Nogle gange (5–29 %) | I 1 tilstand |
| HNF1BHNF1 homeobox B | Nogle gange (5–29 %) | I 2 tilstande |
| HOXD13homeobox D13 | Nogle gange (5–29 %) | I 1 tilstand |
| HSPG2heparan sulfate proteoglycan 2 | Nogle gange (5–29 %) | I 1 tilstand |
| JMJD1Cjumonji domain containing 1C | Nogle gange (5–29 %) | I 1 tilstand |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Nogle gange (5–29 %) | I 1 tilstand |
| KDM1Alysine demethylase 1A | Nogle gange (5–29 %) | I 1 tilstand |
| KDM3Blysine demethylase 3B | Nogle gange (5–29 %) | I 1 tilstand |
| KDM6Alysine demethylase 6A | Nogle gange (5–29 %) | I 1 tilstand |
| KIAA0586KIAA0586 | Nogle gange (5–29 %) | I 1 tilstand |
| KIAA0753KIAA0753 | Nogle gange (5–29 %) | I 1 tilstand |
| KIFBPkinesin family binding protein | Nogle gange (5–29 %) | I 1 tilstand |
| KLHL40kelch like family member 40 | Nogle gange (5–29 %) | I 1 tilstand |
| KLHL41kelch like family member 41 | Nogle gange (5–29 %) | I 1 tilstand |
| KMT2Dlysine methyltransferase 2D | Nogle gange (5–29 %) | I 1 tilstand |
| KRASKRas proto-oncogene, GTPase | Nogle gange (5–29 %) | I 1 tilstand |
| LFNGLFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Nogle gange (5–29 %) | I 1 tilstand |
| LMNAlamin A/C | Nogle gange (5–29 %) | I 1 tilstand |
| LMOD3leiomodin 3 | Nogle gange (5–29 %) | I 1 tilstand |
| LRPPRCleucine rich pentatricopeptide repeat containing | Nogle gange (5–29 %) | I 1 tilstand |
| LUZP1leucine zipper protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MAB21L2mab-21 like 2 | Nogle gange (5–29 %) | I 1 tilstand |
| MAD2L2mitotic arrest deficient 2 like 2 | Nogle gange (5–29 %) | I 1 tilstand |
| MAP2K1mitogen-activated protein kinase kinase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MAPRE2microtubule associated protein RP/EB family member 2 | Nogle gange (5–29 %) | I 2 tilstande |
| MARK2microtubule affinity regulating kinase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Nogle gange (5–29 %) | I 1 tilstand |
| MED12Lmediator complex subunit 12L | Nogle gange (5–29 %) | I 1 tilstand |
| MESP2mesoderm posterior bHLH transcription factor 2 | Nogle gange (5–29 %) | I 1 tilstand |
| MMP23Bmatrix metallopeptidase 23B | Nogle gange (5–29 %) | I 1 tilstand |
| NDUFA6NADH:ubiquinone oxidoreductase subunit A6 | Nogle gange (5–29 %) | I 1 tilstand |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Nogle gange (5–29 %) | I 2 tilstande |
| NEBnebulin | Nogle gange (5–29 %) | I 2 tilstande |
| NOTCH2notch receptor 2 | Nogle gange (5–29 %) | I 2 tilstande |
| OBSL1obscurin like cytoskeletal adaptor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ORC1origin recognition complex subunit 1 | Nogle gange (5–29 %) | I 1 tilstand |
| ORC4origin recognition complex subunit 4 | Nogle gange (5–29 %) | I 1 tilstand |
| ORC6origin recognition complex subunit 6 | Nogle gange (5–29 %) | I 2 tilstande |
| PALB2partner and localizer of BRCA2 | Nogle gange (5–29 %) | I 1 tilstand |
| PDE4Dphosphodiesterase 4D | Nogle gange (5–29 %) | I 2 tilstande |
| PDPNpodoplanin | Nogle gange (5–29 %) | I 1 tilstand |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Nogle gange (5–29 %) | I 2 tilstande |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Nogle gange (5–29 %) | I 1 tilstand |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Nogle gange (5–29 %) | I 1 tilstand |
| PITX2paired like homeodomain 2 | Nogle gange (5–29 %) | I 2 tilstande |
| POLR3ARNA polymerase III subunit A | Nogle gange (5–29 %) | I 2 tilstande |
| PORcytochrome p450 oxidoreductase | Nogle gange (5–29 %) | I 2 tilstande |
| POU6F2POU class 6 homeobox 2 | Nogle gange (5–29 %) | I 1 tilstand |
| PQBP1polyglutamine binding protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| PRDM16PR/SET domain 16 | Nogle gange (5–29 %) | I 1 tilstand |
| PRKCZprotein kinase C zeta | Nogle gange (5–29 %) | I 1 tilstand |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Nogle gange (5–29 %) | I 1 tilstand |
| PSPHphosphoserine phosphatase | Nogle gange (5–29 %) | I 1 tilstand |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Nogle gange (5–29 %) | I 3 tilstande |
| PUF60poly(U) binding splicing factor 60 | Nogle gange (5–29 %) | I 1 tilstand |
| RAD51RAD51 recombinase | Nogle gange (5–29 %) | I 1 tilstand |
| RAD51CRAD51 paralog C | Nogle gange (5–29 %) | I 1 tilstand |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Nogle gange (5–29 %) | I 1 tilstand |
| REREarginine-glutamic acid dipeptide repeats | Nogle gange (5–29 %) | I 3 tilstande |
| RESTRE1 silencing transcription factor | Nogle gange (5–29 %) | I 1 tilstand |
| RFWD3ring finger and WD repeat domain 3 | Nogle gange (5–29 %) | I 1 tilstand |
| RIPPLY2ripply transcriptional repressor 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ROR2ROR family WNT receptor 2 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL11ribosomal protein L11 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL15ribosomal protein L15 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL18ribosomal protein L18 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL26ribosomal protein L26 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL27ribosomal protein L27 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL31ribosomal protein L31 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL35ribosomal protein L35 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL35Aribosomal protein L35a | Nogle gange (5–29 %) | I 2 tilstande |
| RPL5ribosomal protein L5 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL8ribosomal protein L8 | Nogle gange (5–29 %) | I 1 tilstand |
| RPL9ribosomal protein L9 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS10ribosomal protein S10 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS15Aribosomal protein S15a | Nogle gange (5–29 %) | I 1 tilstand |
| RPS17ribosomal protein S17 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS19ribosomal protein S19 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS20ribosomal protein S20 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS24ribosomal protein S24 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS26ribosomal protein S26 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS27ribosomal protein S27 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS28ribosomal protein S28 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS29ribosomal protein S29 | Nogle gange (5–29 %) | I 1 tilstand |
| RPS7ribosomal protein S7 | Nogle gange (5–29 %) | I 1 tilstand |
| RREB1ras responsive element binding protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| RTTNrotatin | Nogle gange (5–29 %) | I 1 tilstand |
| SALL1spalt like transcription factor 1 | Nogle gange (5–29 %) | I 2 tilstande |
| SCUBE3signal peptide, CUB domain and EGF like domain containing 3 | Nogle gange (5–29 %) | I 1 tilstand |
| SEC24CSEC24 homolog C, COPII component | Nogle gange (5–29 %) | I 1 tilstand |
| SIN3ASIN3 transcription regulator family member A | Nogle gange (5–29 %) | I 2 tilstande |
| SKISKI proto-oncogene | Nogle gange (5–29 %) | I 1 tilstand |
| SKIC3SKI3 subunit of superkiller complex | Nogle gange (5–29 %) | I 1 tilstand |
| SLX4SLX4 structure-specific endonuclease subunit | Nogle gange (5–29 %) | I 1 tilstand |
| SMAD4SMAD family member 4 | Nogle gange (5–29 %) | I 1 tilstand |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SMARCA4SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4 | Nogle gange (5–29 %) | I 1 tilstand |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Nogle gange (5–29 %) | I 1 tilstand |
| SMARCC2SWI/SNF related BAF chromatin remodeling complex subunit C2 | Nogle gange (5–29 %) | I 1 tilstand |
| SMARCD1SWI/SNF related BAF chromatin remodeling complex subunit D1 | Nogle gange (5–29 %) | I 1 tilstand |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Nogle gange (5–29 %) | I 1 tilstand |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SMSspermine synthase | Nogle gange (5–29 %) | I 1 tilstand |
| SOX11SRY-box transcription factor 11 | Nogle gange (5–29 %) | I 1 tilstand |
| SOX2SRY-box transcription factor 2 | Nogle gange (5–29 %) | I 2 tilstande |
| SOX4SRY-box transcription factor 4 | Nogle gange (5–29 %) | I 1 tilstand |
| SPENspen family transcriptional repressor | Nogle gange (5–29 %) | I 1 tilstand |
| SRCAPSnf2 related CREBBP activator protein | Nogle gange (5–29 %) | I 2 tilstande |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TBX1T-box transcription factor 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TBX6T-box transcription factor 6 | Nogle gange (5–29 %) | I 1 tilstand |
| TCF12transcription factor 12 | Nogle gange (5–29 %) | I 1 tilstand |
| THOC6THO complex subunit 6 | Nogle gange (5–29 %) | I 1 tilstand |
| TMEM94transmembrane protein 94 | Nogle gange (5–29 %) | I 1 tilstand |
| TONSLtonsoku like, DNA repair protein | Nogle gange (5–29 %) | I 1 tilstand |
| TRIM28tripartite motif containing 28 | Nogle gange (5–29 %) | I 1 tilstand |
| TRIP13thyroid hormone receptor interactor 13 | Nogle gange (5–29 %) | I 1 tilstand |
| TSR2TSR2 ribosome maturation factor | Nogle gange (5–29 %) | I 1 tilstand |
| TUBBtubulin beta class I | Nogle gange (5–29 %) | I 1 tilstand |
| UBE2Aubiquitin conjugating enzyme E2 A | Nogle gange (5–29 %) | I 1 tilstand |
| UBE2Tubiquitin conjugating enzyme E2 T | Nogle gange (5–29 %) | I 1 tilstand |
| UBE4Bubiquitination factor E4B | Nogle gange (5–29 %) | I 1 tilstand |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Nogle gange (5–29 %) | I 2 tilstande |
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Nogle gange (5–29 %) | I 1 tilstand |
| USP9Xubiquitin specific peptidase 9 X-linked | Nogle gange (5–29 %) | I 1 tilstand |
| VPS35LVPS35 endosomal protein sorting factor like | Nogle gange (5–29 %) | I 1 tilstand |
| WASHC5WASH complex subunit 5 | Nogle gange (5–29 %) | I 2 tilstande |
| WNT5AWnt family member 5A | Nogle gange (5–29 %) | I 1 tilstand |
| XRCC2X-ray repair cross complementing 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ZMPSTE24zinc metallopeptidase STE24 | Nogle gange (5–29 %) | I 2 tilstande |
| ZMYM2zinc finger MYM-type containing 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ZNF699zinc finger protein 699 | Nogle gange (5–29 %) | I 1 tilstand |
| ACBD6acyl-CoA binding domain containing 6 | Sjældent (1–4%) | I 1 tilstand |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Sjældent (1–4%) | I 1 tilstand |
| APC2APC regulator of Wnt signaling pathway 2 | Sjældent (1–4%) | I 1 tilstand |
| EHMT1euchromatic histone lysine methyltransferase 1 | Sjældent (1–4%) | I 1 tilstand |
| MTORmechanistic target of rapamycin kinase | Sjældent (1–4%) | I 1 tilstand |
| NKX2-1NK2 homeobox 1 | Sjældent (1–4%) | I 1 tilstand |
| NSD1nuclear receptor binding SET domain protein 1 | Sjældent (1–4%) | I 1 tilstand |
| SETBP1SET binding protein 1 | Sjældent (1–4%) | I 2 tilstande |
| SPTBN1spectrin beta, non-erythrocytic 1 | Sjældent (1–4%) | I 1 tilstand |
| SUCLG1succinate-CoA ligase GDP/ADP-forming subunit alpha | Sjældent (1–4%) | I 1 tilstand |
| ATRATR checkpoint kinase | Ikke registreret | I 1 tilstand |
| ATRXATRX chromatin remodeler | Ikke registreret | I 2 tilstande |
| BUB1BBUB1 mitotic checkpoint serine/threonine kinase B | Ikke registreret | I 1 tilstand |
| CARS1cysteinyl-tRNA synthetase 1 | Ikke registreret | I 1 tilstand |
| CDCA7cell division cycle associated 7 | Ikke registreret | I 1 tilstand |
| CHRNGcholinergic receptor nicotinic gamma subunit | Ikke registreret | I 1 tilstand |
| CUL4Bcullin 4B | Ikke registreret | I 1 tilstand |
| CYP21A2cytochrome P450 family 21 subfamily A member 2 | Ikke registreret | I 1 tilstand |
| DKC1dyskerin pseudouridine synthase 1 | Ikke registreret | I 1 tilstand |
| FGFR1fibroblast growth factor receptor 1 | Ikke registreret | I 2 tilstande |
| HUWE1HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1 | Ikke registreret | I 1 tilstand |
| HYLS1HYLS1 centriolar and ciliogenesis associated | Ikke registreret | I 1 tilstand |
| PCNTpericentrin | Ikke registreret | I 1 tilstand |
| RBBP8RB binding protein 8, endonuclease | Ikke registreret | I 1 tilstand |
| RLIMring finger protein, LIM domain interacting | Ikke registreret | I 1 tilstand |
| RSPO1R-spondin 1 | Ikke registreret | I 1 tilstand |
| SETD5SET domain containing 5 | Ikke registreret | I 1 tilstand |
| SIX6SIX homeobox 6 | Ikke registreret | I 1 tilstand |
| SSR4signal sequence receptor subunit 4 | Ikke registreret | I 1 tilstand |
| STARsteroidogenic acute regulatory protein | Ikke registreret | I 1 tilstand |
| TAPT1transmembrane anterior posterior transformation 1 | Ikke registreret | I 1 tilstand |
| TFAP2Atranscription factor AP-2 alpha | Ikke registreret | I 1 tilstand |
| TTC8tetratricopeptide repeat domain 8 | Ikke registreret | I 1 tilstand |
| UBA1ubiquitin like modifier activating enzyme 1 | Ikke registreret | I 1 tilstand |
| WDR35WD repeat domain 35 | Ikke registreret | I 1 tilstand |
| WNT7AWnt family member 7A | Ikke registreret | I 1 tilstand |
| ZMIZ1zinc finger MIZ-type containing 1 | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
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Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.19-9814e911.
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