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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.
Podsumowanie
- Znana także jako
- Hypospadia
- Układ organizmu
- Abnormality of the genitourinary system
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Zaloguj sięZapytajZsekwencjonuj swój genom↗
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Aby odczytać ją jako JSON, dodaj .json na końcu adresu strony lub zażądaj application/json.
library(jsonlite)
url <- "https://dantelabs.com/traits/hypospadias.json"
page <- fromJSON(url)
page$trait$nameHypospadiasHP:0000047
AtlasDla kogo jest Dante LabsNasza naukaProduktyWyniki
Zaloguj sięZapytajZsekwencjonuj swój genom↗
Odczytaj geny powiązane z Hypospadias oraz resztę swojego genomu za pomocą jednego badania.
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Zamawiam Genome Test160 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 156 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 →
- Myelodysplastic Syndrome (MDS)Reads 1 of these genesSAMD9About 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 →
Odczytaj geny powiązane z Hypospadias oraz resztę swojego genomu za pomocą jednego badania.
Od 449 $Bezpłatna wysyłka · Wyniki w ciągu 6–8 tygodni
Zamawiam Genome Test384 genów powiązanych z Hypospadias
Zmiany w tych genach powodują rzadkie choroby, w których występuje Hypospadias. Większość osób z tą cechą nie ma żadnej z tych chorób, a gen z tej listy nic nie mówi o czyimkolwiek własnym genomie.
| Gen | Jak często występuje | Choroby |
|---|---|---|
| B9D2B9 domain containing 2 | Zawsze | W 1 chorobie |
| CACHD1cache domain containing 1 | Zawsze | W 1 chorobie |
| CDH11cadherin 11 | Zawsze | W 2 chorobach |
| DHRS3dehydrogenase/reductase 3 | Zawsze | W 1 chorobie |
| FGFR2fibroblast growth factor receptor 2 | Zawsze | W 1 chorobie |
| FRYLFRY like transcription coactivator | Zawsze | W 1 chorobie |
| H4C11H4 clustered histone 11 | Zawsze | W 1 chorobie |
| IKZF2IKAROS family zinc finger 2 | Zawsze | W 1 chorobie |
| JKAMPJNK1/MAPK8 associated membrane protein | Zawsze | W 1 chorobie |
| KLF1KLF transcription factor 1 | Zawsze | W 2 chorobach |
| MAN2B2mannosidase alpha class 2B member 2 | Zawsze | W 1 chorobie |
| MED25mediator complex subunit 25 | Zawsze | W 2 chorobach |
| MSL2MSL complex subunit 2 | Zawsze | W 1 chorobie |
| NDUFA8NADH:ubiquinone oxidoreductase subunit A8 | Zawsze | W 1 chorobie |
| NDUFB7NADH:ubiquinone oxidoreductase subunit B7 | Zawsze | W 1 chorobie |
| NDUFS4NADH:ubiquinone oxidoreductase subunit S4 | Zawsze | W 1 chorobie |
| PPP1R12Aprotein phosphatase 1 regulatory subunit 12A | Zawsze | W 1 chorobie |
| PRPS1phosphoribosyl pyrophosphate synthetase 1 | Zawsze | W 1 chorobie |
| PTBP1polypyrimidine tract binding protein 1 | Zawsze | W 1 chorobie |
| RNU12RNA, U12 small nuclear | Zawsze | W 2 chorobach |
| RNU5B-1RNA, U5B small nuclear 1 | Zawsze | W 1 chorobie |
| SAMD9sterile alpha motif domain containing 9 | Zawsze | W 1 chorobie |
| SLC25A10solute carrier family 25 member 10 | Zawsze | W 1 chorobie |
| SOX9SRY-box transcription factor 9 | Zawsze | W 4 chorobach |
| TOP2BDNA topoisomerase II beta | Zawsze | W 1 chorobie |
| ZMYM3zinc finger MYM-type containing 3 | Zawsze | W 1 chorobie |
| CDKN1Ccyclin dependent kinase inhibitor 1C | Bardzo często (80–99%) | W 3 chorobach |
| CPLX1complexin 1 | Bardzo często (80–99%) | W 2 chorobach |
| CTBP1C-terminal binding protein 1 | Bardzo często (80–99%) | W 2 chorobach |
| CUL7cullin 7 | Bardzo często (80–99%) | W 2 chorobach |
| CYB5Acytochrome b5 type A | Bardzo często (80–99%) | W 2 chorobach |
| CYP17A1cytochrome P450 family 17 subfamily A member 1 | Bardzo często (80–99%) | W 2 chorobach |
| DHX37DEAH-box helicase 37 | Bardzo często (80–99%) | W 1 chorobie |
| GATA4GATA binding protein 4 | Bardzo często (80–99%) | W 2 chorobach |
| HSD17B3hydroxysteroid 17-beta dehydrogenase 3 | Bardzo często (80–99%) | W 1 chorobie |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Bardzo często (80–99%) | W 2 chorobach |
| MAP3K1mitogen-activated protein kinase kinase kinase 1 | Bardzo często (80–99%) | W 2 chorobach |
| MECP2methyl-CpG binding protein 2 | Bardzo często (80–99%) | W 2 chorobach |
| MID1midline 1 | Bardzo często (80–99%) | W 2 chorobach |
| NELFAnegative elongation factor complex member A | Bardzo często (80–99%) | W 1 chorobie |
Pokaż jeszcze 344 genów
| Gen | Jak często występuje | Choroby |
|---|---|---|
| NR0B1nuclear receptor subfamily 0 group B member 1 | Bardzo często (80–99%) | W 1 chorobie |
| NR5A1nuclear receptor subfamily 5 group A member 1 | Bardzo często (80–99%) | W 2 chorobach |
| NSD2nuclear receptor binding SET domain protein 2 | Bardzo często (80–99%) | W 2 chorobach |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Bardzo często (80–99%) | W 1 chorobie |
| POLEDNA polymerase epsilon, catalytic subunit | Bardzo często (80–99%) | W 2 chorobach |
| SRYsex determining region Y | Bardzo często (80–99%) | W 4 chorobach |
| TBX22T-box transcription factor 22 | Bardzo często (80–99%) | W 2 chorobach |
| TSHZ3teashirt zinc finger homeobox 3 | Bardzo często (80–99%) | W 1 chorobie |
| VAMP7vesicle associated membrane protein 7 | Bardzo często (80–99%) | W 1 chorobie |
| WT1WT1 transcription factor | Bardzo często (80–99%) | W 3 chorobach |
| WWOXWW domain containing oxidoreductase | Bardzo często (80–99%) | W 1 chorobie |
| ZFPM2zinc finger protein, FOG family member 2 | Bardzo często (80–99%) | W 1 chorobie |
| ABL1ABL proto-oncogene 1, non-receptor tyrosine kinase | Często (30–79%) | W 1 chorobie |
| ARandrogen receptor | Często (30–79%) | W 1 chorobie |
| ATP6AP2ATPase H+ transporting accessory protein 2 | Często (30–79%) | W 1 chorobie |
| B3GLCTbeta 3-glucosyltransferase | Często (30–79%) | W 2 chorobach |
| BBS2Bardet-Biedl syndrome 2 | Często (30–79%) | W 1 chorobie |
| BCORBCL6 corepressor | Często (30–79%) | W 3 chorobach |
| BRD4bromodomain containing 4 | Często (30–79%) | W 1 chorobie |
| CHRNA3cholinergic receptor nicotinic alpha 3 subunit | Często (30–79%) | W 1 chorobie |
| COG1component of oligomeric golgi complex 1 | Często (30–79%) | W 1 chorobie |
| CREBBPCREB binding lysine acetyltransferase | Często (30–79%) | W 3 chorobach |
| DACT1dishevelled binding antagonist of beta catenin 1 | Często (30–79%) | W 2 chorobach |
| DHCR77-dehydrocholesterol reductase | Często (30–79%) | W 2 chorobach |
| DNAJC19DnaJ heat shock protein family (Hsp40) member C19 | Często (30–79%) | W 1 chorobie |
| DOT1LDOT1 like histone lysine methyltransferase | Często (30–79%) | W 1 chorobie |
| DVL1dishevelled segment polarity protein 1 | Często (30–79%) | W 2 chorobach |
| DYNC2LI1dynein cytoplasmic 2 light intermediate chain 1 | Często (30–79%) | W 1 chorobie |
| EP300EP300 lysine acetyltransferase | Często (30–79%) | W 2 chorobach |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Często (30–79%) | W 2 chorobach |
| EVCEvC ciliary complex subunit 1 | Często (30–79%) | W 2 chorobach |
| EVC2EvC ciliary complex subunit 2 | Często (30–79%) | W 2 chorobach |
| FDFT1farnesyl-diphosphate farnesyltransferase 1 | Często (30–79%) | W 1 chorobie |
| FGFRL1fibroblast growth factor receptor like 1 | Często (30–79%) | W 1 chorobie |
| FIG4FIG4 phosphoinositide 5-phosphatase | Często (30–79%) | W 2 chorobach |
| FLNAfilamin A | Często (30–79%) | W 2 chorobach |
| GINS3GINS complex subunit 3 | Często (30–79%) | W 1 chorobie |
| GLI1GLI family zinc finger 1 | Często (30–79%) | W 1 chorobie |
| HDAC8histone deacetylase 8 | Często (30–79%) | W 1 chorobie |
| HMGA2high mobility group AT-hook 2 | Często (30–79%) | W 1 chorobie |
| HNRNPH1heterogeneous nuclear ribonucleoprotein H1 | Często (30–79%) | W 1 chorobie |
| HOXA13homeobox A13 | Często (30–79%) | W 2 chorobach |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Często (30–79%) | W 2 chorobach |
| IGF2insulin like growth factor 2 | Często (30–79%) | W 2 chorobach |
| KAT5lysine acetyltransferase 5 | Często (30–79%) | W 1 chorobie |
| KAT6Blysine acetyltransferase 6B | Często (30–79%) | W 1 chorobie |
| KDM5Blysine demethylase 5B | Często (30–79%) | W 1 chorobie |
| KIF7kinesin family member 7 | Często (30–79%) | W 2 chorobach |
| LSM7LSM7 homolog, U6 small nuclear RNA and mRNA degradation associated | Często (30–79%) | W 1 chorobie |
| LSSlanosterol synthase | Często (30–79%) | W 1 chorobie |
| MAB21L1mab-21 like 1 | Często (30–79%) | W 1 chorobie |
| MAU2MAU2 sister chromatid cohesion factor | Często (30–79%) | W 1 chorobie |
| MAXMYC associated transcriptional regulator X | Często (30–79%) | W 1 chorobie |
| MCTP2multiple C2 and transmembrane domain containing 2 | Często (30–79%) | W 1 chorobie |
| MED12mediator complex subunit 12 | Często (30–79%) | W 1 chorobie |
| MKKSMKKS centrosomal shuttling protein | Często (30–79%) | W 1 chorobie |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Często (30–79%) | W 2 chorobach |
| NIPBLNIPBL cohesin loading factor | Często (30–79%) | W 2 chorobach |
| OGTO-linked N-acetylglucosamine (GlcNAc) transferase | Często (30–79%) | W 1 chorobie |
| OTUD5OTU deubiquitinase 5 | Często (30–79%) | W 1 chorobie |
| PAX6paired box 6 | Często (30–79%) | W 1 chorobie |
| PEX1peroxisomal biogenesis factor 1 | Często (30–79%) | W 2 chorobach |
| PEX10peroxisomal biogenesis factor 10 | Często (30–79%) | W 1 chorobie |
| PEX11Bperoxisomal biogenesis factor 11 beta | Często (30–79%) | W 1 chorobie |
| PEX12peroxisomal biogenesis factor 12 | Często (30–79%) | W 1 chorobie |
| PEX13peroxisomal biogenesis factor 13 | Często (30–79%) | W 1 chorobie |
| PEX14peroxisomal biogenesis factor 14 | Często (30–79%) | W 1 chorobie |
| PEX16peroxisomal biogenesis factor 16 | Często (30–79%) | W 1 chorobie |
| PEX19peroxisomal biogenesis factor 19 | Często (30–79%) | W 1 chorobie |
| PEX2peroxisomal biogenesis factor 2 | Często (30–79%) | W 2 chorobach |
| PEX26peroxisomal biogenesis factor 26 | Często (30–79%) | W 1 chorobie |
| PEX3peroxisomal biogenesis factor 3 | Często (30–79%) | W 1 chorobie |
| PEX5peroxisomal biogenesis factor 5 | Często (30–79%) | W 1 chorobie |
| PEX6peroxisomal biogenesis factor 6 | Często (30–79%) | W 1 chorobie |
| PLAG1PLAG1 zinc finger | Często (30–79%) | W 1 chorobie |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Często (30–79%) | W 1 chorobie |
| PRKACBprotein kinase cAMP-activated catalytic subunit beta | Często (30–79%) | W 1 chorobie |
| PTDSS1phosphatidylserine synthase 1 | Często (30–79%) | W 2 chorobach |
| PUM1pumilio RNA binding family member 1 | Często (30–79%) | W 1 chorobie |
| RAC1Rac family small GTPase 1 | Często (30–79%) | W 2 chorobach |
| RAD21RAD21 cohesin complex component | Często (30–79%) | W 1 chorobie |
| RPL10ribosomal protein L10 | Często (30–79%) | W 3 chorobach |
| SIAH1siah E3 ubiquitin protein ligase 1 | Często (30–79%) | W 1 chorobie |
| SMC1Astructural maintenance of chromosomes 1A | Często (30–79%) | W 1 chorobie |
| SMC3structural maintenance of chromosomes 3 | Często (30–79%) | W 1 chorobie |
| SMG8SMG8 nonsense mediated mRNA decay factor | Często (30–79%) | W 1 chorobie |
| TMEM63Atransmembrane protein 63A | Często (30–79%) | W 1 chorobie |
| TMEM70transmembrane protein 70 | Często (30–79%) | W 2 chorobach |
| TP63tumor protein p63 | Często (30–79%) | W 3 chorobach |
| TRIM8tripartite motif containing 8 | Często (30–79%) | W 1 chorobie |
| VAC14VAC14 component of PIKFYVE complex | Często (30–79%) | W 1 chorobie |
| WBP4WW domain binding protein 4 | Często (30–79%) | W 1 chorobie |
| WNT4Wnt family member 4 | Często (30–79%) | W 2 chorobach |
| ZEB2zinc finger E-box binding homeobox 2 | Często (30–79%) | W 3 chorobach |
| ZFXzinc finger protein X-linked | Często (30–79%) | W 1 chorobie |
| ACTA1actin alpha 1, skeletal muscle | Czasami (5–29%) | W 1 chorobie |
| ADA2adenosine deaminase 2 | Czasami (5–29%) | W 1 chorobie |
| ADAT3adenosine deaminase tRNA specific 3 | Czasami (5–29%) | W 1 chorobie |
| AFF4ALF transcription elongation factor 4 | Czasami (5–29%) | W 1 chorobie |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Czasami (5–29%) | W 2 chorobach |
| ARID1AAT-rich interaction domain 1A | Czasami (5–29%) | W 1 chorobie |
| ARID1BAT-rich interaction domain 1B | Czasami (5–29%) | W 2 chorobach |
| ARID2AT-rich interaction domain 2 | Czasami (5–29%) | W 1 chorobie |
| ARVCFARVCF delta catenin family member | Czasami (5–29%) | W 1 chorobie |
| ARXaristaless related homeobox | Czasami (5–29%) | W 2 chorobach |
| BICRABRD4 interacting chromatin remodeling complex associated protein | Czasami (5–29%) | W 1 chorobie |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Czasami (5–29%) | W 2 chorobach |
| BRCA1BRCA1 DNA repair associated | Czasami (5–29%) | W 1 chorobie |
| BRCA2BRCA2 DNA repair associated | Czasami (5–29%) | W 2 chorobach |
| BRIP1BRCA1 interacting DNA helicase 1 | Czasami (5–29%) | W 1 chorobie |
| CASZ1castor zinc finger 1 | Czasami (5–29%) | W 1 chorobie |
| CCDC22CCC complex scaffolding subunit CCDC22 | Czasami (5–29%) | W 1 chorobie |
| CCDC8coiled-coil domain containing 8 subunit of 3M complex | Czasami (5–29%) | W 1 chorobie |
| CDC42cell division cycle 42 | Czasami (5–29%) | W 2 chorobach |
| CDC42BPBCDC42 binding protein kinase beta | Czasami (5–29%) | W 1 chorobie |
| CDC45cell division cycle 45 | Czasami (5–29%) | W 2 chorobach |
| CDC6cell division cycle 6 | Czasami (5–29%) | W 1 chorobie |
| CDT1chromatin licensing and DNA replication factor 1 | Czasami (5–29%) | W 1 chorobie |
| CEP152centrosomal protein 152 | Czasami (5–29%) | W 1 chorobie |
| CILK1ciliogenesis associated kinase 1 | Czasami (5–29%) | W 1 chorobie |
| COL3A1collagen type III alpha 1 chain | Czasami (5–29%) | W 1 chorobie |
| COLEC11collectin subfamily member 11 | Czasami (5–29%) | W 1 chorobie |
| COMTcatechol-O-methyltransferase | Czasami (5–29%) | W 1 chorobie |
| COX7Bcytochrome c oxidase subunit 7B | Czasami (5–29%) | W 2 chorobach |
| CSPP1centrosome and spindle pole associated protein 1 | Czasami (5–29%) | W 1 chorobie |
| CTR9CTR9 component of Paf1/RNA polymerase II complex | Czasami (5–29%) | W 1 chorobie |
| CUX1cut like homeobox 1 | Czasami (5–29%) | W 1 chorobie |
| DCHS1dachsous cadherin-related 1 | Czasami (5–29%) | W 2 chorobach |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Czasami (5–29%) | W 1 chorobie |
| DLL3delta like canonical Notch ligand 3 | Czasami (5–29%) | W 1 chorobie |
| DPF2double PHD fingers 2 | Czasami (5–29%) | W 1 chorobie |
| DPP9dipeptidyl peptidase 9 | Czasami (5–29%) | W 1 chorobie |
| DPYSL5dihydropyrimidinase like 5 | Czasami (5–29%) | W 1 chorobie |
| DVL3dishevelled segment polarity protein 3 | Czasami (5–29%) | W 1 chorobie |
| DYRK1Adual specificity tyrosine phosphorylation regulated kinase 1A | Czasami (5–29%) | W 2 chorobach |
| EFNB1ephrin B1 | Czasami (5–29%) | W 2 chorobach |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Czasami (5–29%) | W 1 chorobie |
| ERMARDER membrane associated RNA degradation | Czasami (5–29%) | W 1 chorobie |
| FAAP100FA core complex associated protein 100 | Czasami (5–29%) | W 1 chorobie |
| FANCAFA complementation group A | Czasami (5–29%) | W 1 chorobie |
| FANCBFA complementation group B | Czasami (5–29%) | W 1 chorobie |
| FANCCFA complementation group C | Czasami (5–29%) | W 1 chorobie |
| FANCD2FA complementation group D2 | Czasami (5–29%) | W 1 chorobie |
| FANCEFA complementation group E | Czasami (5–29%) | W 1 chorobie |
| FANCFFA complementation group F | Czasami (5–29%) | W 1 chorobie |
| FANCGFA complementation group G | Czasami (5–29%) | W 1 chorobie |
| FANCIFA complementation group I | Czasami (5–29%) | W 1 chorobie |
| FANCLFA complementation group L | Czasami (5–29%) | W 1 chorobie |
| FANCMFA complementation group M | Czasami (5–29%) | W 1 chorobie |
| FAT4FAT atypical cadherin 4 | Czasami (5–29%) | W 2 chorobach |
| FBXL4F-box and leucine rich repeat protein 4 | Czasami (5–29%) | W 1 chorobie |
| FGD1FYVE, RhoGEF and PH domain containing 1 | Czasami (5–29%) | W 1 chorobie |
| FOCADfocadhesin | Czasami (5–29%) | W 1 chorobie |
| FOXC1forkhead box C1 | Czasami (5–29%) | W 1 chorobie |
| FOXF1forkhead box F1 | Czasami (5–29%) | W 1 chorobie |
| FRAS1Fraser extracellular matrix complex subunit 1 | Czasami (5–29%) | W 2 chorobach |
| FREM2FRAS1 related extracellular matrix 2 | Czasami (5–29%) | W 1 chorobie |
| FZD2frizzled class receptor 2 | Czasami (5–29%) | W 2 chorobach |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Czasami (5–29%) | W 1 chorobie |
| GATA1GATA binding protein 1 | Czasami (5–29%) | W 1 chorobie |
| GATAD2BGATA zinc finger domain containing 2B | Czasami (5–29%) | W 1 chorobie |
| GFM1G elongation factor mitochondrial 1 | Czasami (5–29%) | W 1 chorobie |
| GLI3GLI family zinc finger 3 | Czasami (5–29%) | W 4 chorobach |
| GMNNgeminin DNA replication inhibitor | Czasami (5–29%) | W 1 chorobie |
| GP1BBglycoprotein Ib platelet subunit beta | Czasami (5–29%) | W 1 chorobie |
| GPC3glypican 3 | Czasami (5–29%) | W 3 chorobach |
| GPC4glypican 4 | Czasami (5–29%) | W 1 chorobie |
| GRB10growth factor receptor bound protein 10 | Czasami (5–29%) | W 1 chorobie |
| GRIP1glutamate receptor interacting protein 1 | Czasami (5–29%) | W 1 chorobie |
| H19H19 imprinted maternally expressed transcript | Czasami (5–29%) | W 1 chorobie |
| HBA1hemoglobin subunit alpha 1 | Czasami (5–29%) | W 1 chorobie |
| HBA2hemoglobin subunit alpha 2 | Czasami (5–29%) | W 1 chorobie |
| HCCSholocytochrome c synthase | Czasami (5–29%) | W 2 chorobach |
| HEATR3HEAT repeat containing 3 | Czasami (5–29%) | W 1 chorobie |
| HES7hes family bHLH transcription factor 7 | Czasami (5–29%) | W 1 chorobie |
| HIRAhistone cell cycle regulator | Czasami (5–29%) | W 1 chorobie |
| HNF1BHNF1 homeobox B | Czasami (5–29%) | W 2 chorobach |
| HOXD13homeobox D13 | Czasami (5–29%) | W 1 chorobie |
| HSPG2heparan sulfate proteoglycan 2 | Czasami (5–29%) | W 1 chorobie |
| JMJD1Cjumonji domain containing 1C | Czasami (5–29%) | W 1 chorobie |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Czasami (5–29%) | W 1 chorobie |
| KDM1Alysine demethylase 1A | Czasami (5–29%) | W 1 chorobie |
| KDM3Blysine demethylase 3B | Czasami (5–29%) | W 1 chorobie |
| KDM6Alysine demethylase 6A | Czasami (5–29%) | W 1 chorobie |
| KIAA0586KIAA0586 | Czasami (5–29%) | W 1 chorobie |
| KIAA0753KIAA0753 | Czasami (5–29%) | W 1 chorobie |
| KIFBPkinesin family binding protein | Czasami (5–29%) | W 1 chorobie |
| KLHL40kelch like family member 40 | Czasami (5–29%) | W 1 chorobie |
| KLHL41kelch like family member 41 | Czasami (5–29%) | W 1 chorobie |
| KMT2Dlysine methyltransferase 2D | Czasami (5–29%) | W 1 chorobie |
| KRASKRas proto-oncogene, GTPase | Czasami (5–29%) | W 1 chorobie |
| LFNGLFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | Czasami (5–29%) | W 1 chorobie |
| LMNAlamin A/C | Czasami (5–29%) | W 1 chorobie |
| LMOD3leiomodin 3 | Czasami (5–29%) | W 1 chorobie |
| LRPPRCleucine rich pentatricopeptide repeat containing | Czasami (5–29%) | W 1 chorobie |
| LUZP1leucine zipper protein 1 | Czasami (5–29%) | W 1 chorobie |
| MAB21L2mab-21 like 2 | Czasami (5–29%) | W 1 chorobie |
| MAD2L2mitotic arrest deficient 2 like 2 | Czasami (5–29%) | W 1 chorobie |
| MAP2K1mitogen-activated protein kinase kinase 1 | Czasami (5–29%) | W 1 chorobie |
| MAPRE2microtubule associated protein RP/EB family member 2 | Czasami (5–29%) | W 2 chorobach |
| MARK2microtubule affinity regulating kinase 2 | Czasami (5–29%) | W 1 chorobie |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Czasami (5–29%) | W 1 chorobie |
| MED12Lmediator complex subunit 12L | Czasami (5–29%) | W 1 chorobie |
| MESP2mesoderm posterior bHLH transcription factor 2 | Czasami (5–29%) | W 1 chorobie |
| MMP23Bmatrix metallopeptidase 23B | Czasami (5–29%) | W 1 chorobie |
| NDUFA6NADH:ubiquinone oxidoreductase subunit A6 | Czasami (5–29%) | W 1 chorobie |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Czasami (5–29%) | W 2 chorobach |
| NEBnebulin | Czasami (5–29%) | W 2 chorobach |
| NOTCH2notch receptor 2 | Czasami (5–29%) | W 2 chorobach |
| OBSL1obscurin like cytoskeletal adaptor 1 | Czasami (5–29%) | W 1 chorobie |
| ORC1origin recognition complex subunit 1 | Czasami (5–29%) | W 1 chorobie |
| ORC4origin recognition complex subunit 4 | Czasami (5–29%) | W 1 chorobie |
| ORC6origin recognition complex subunit 6 | Czasami (5–29%) | W 2 chorobach |
| PALB2partner and localizer of BRCA2 | Czasami (5–29%) | W 1 chorobie |
| PDE4Dphosphodiesterase 4D | Czasami (5–29%) | W 2 chorobach |
| PDPNpodoplanin | Czasami (5–29%) | W 1 chorobie |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Czasami (5–29%) | W 2 chorobach |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Czasami (5–29%) | W 1 chorobie |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Czasami (5–29%) | W 1 chorobie |
| PITX2paired like homeodomain 2 | Czasami (5–29%) | W 2 chorobach |
| POLR3ARNA polymerase III subunit A | Czasami (5–29%) | W 2 chorobach |
| PORcytochrome p450 oxidoreductase | Czasami (5–29%) | W 2 chorobach |
| POU6F2POU class 6 homeobox 2 | Czasami (5–29%) | W 1 chorobie |
| PQBP1polyglutamine binding protein 1 | Czasami (5–29%) | W 1 chorobie |
| PRDM16PR/SET domain 16 | Czasami (5–29%) | W 1 chorobie |
| PRKCZprotein kinase C zeta | Czasami (5–29%) | W 1 chorobie |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Czasami (5–29%) | W 1 chorobie |
| PSPHphosphoserine phosphatase | Czasami (5–29%) | W 1 chorobie |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Czasami (5–29%) | W 3 chorobach |
| PUF60poly(U) binding splicing factor 60 | Czasami (5–29%) | W 1 chorobie |
| RAD51RAD51 recombinase | Czasami (5–29%) | W 1 chorobie |
| RAD51CRAD51 paralog C | Czasami (5–29%) | W 1 chorobie |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Czasami (5–29%) | W 1 chorobie |
| REREarginine-glutamic acid dipeptide repeats | Czasami (5–29%) | W 3 chorobach |
| RESTRE1 silencing transcription factor | Czasami (5–29%) | W 1 chorobie |
| RFWD3ring finger and WD repeat domain 3 | Czasami (5–29%) | W 1 chorobie |
| RIPPLY2ripply transcriptional repressor 2 | Czasami (5–29%) | W 1 chorobie |
| ROR2ROR family WNT receptor 2 | Czasami (5–29%) | W 1 chorobie |
| RPL11ribosomal protein L11 | Czasami (5–29%) | W 1 chorobie |
| RPL15ribosomal protein L15 | Czasami (5–29%) | W 1 chorobie |
| RPL18ribosomal protein L18 | Czasami (5–29%) | W 1 chorobie |
| RPL26ribosomal protein L26 | Czasami (5–29%) | W 1 chorobie |
| RPL27ribosomal protein L27 | Czasami (5–29%) | W 1 chorobie |
| RPL31ribosomal protein L31 | Czasami (5–29%) | W 1 chorobie |
| RPL35ribosomal protein L35 | Czasami (5–29%) | W 1 chorobie |
| RPL35Aribosomal protein L35a | Czasami (5–29%) | W 2 chorobach |
| RPL5ribosomal protein L5 | Czasami (5–29%) | W 1 chorobie |
| RPL8ribosomal protein L8 | Czasami (5–29%) | W 1 chorobie |
| RPL9ribosomal protein L9 | Czasami (5–29%) | W 1 chorobie |
| RPS10ribosomal protein S10 | Czasami (5–29%) | W 1 chorobie |
| RPS15Aribosomal protein S15a | Czasami (5–29%) | W 1 chorobie |
| RPS17ribosomal protein S17 | Czasami (5–29%) | W 1 chorobie |
| RPS19ribosomal protein S19 | Czasami (5–29%) | W 1 chorobie |
| RPS20ribosomal protein S20 | Czasami (5–29%) | W 1 chorobie |
| RPS24ribosomal protein S24 | Czasami (5–29%) | W 1 chorobie |
| RPS26ribosomal protein S26 | Czasami (5–29%) | W 1 chorobie |
| RPS27ribosomal protein S27 | Czasami (5–29%) | W 1 chorobie |
| RPS28ribosomal protein S28 | Czasami (5–29%) | W 1 chorobie |
| RPS29ribosomal protein S29 | Czasami (5–29%) | W 1 chorobie |
| RPS7ribosomal protein S7 | Czasami (5–29%) | W 1 chorobie |
| RREB1ras responsive element binding protein 1 | Czasami (5–29%) | W 1 chorobie |
| RTTNrotatin | Czasami (5–29%) | W 1 chorobie |
| SALL1spalt like transcription factor 1 | Czasami (5–29%) | W 2 chorobach |
| SCUBE3signal peptide, CUB domain and EGF like domain containing 3 | Czasami (5–29%) | W 1 chorobie |
| SEC24CSEC24 homolog C, COPII component | Czasami (5–29%) | W 1 chorobie |
| SIN3ASIN3 transcription regulator family member A | Czasami (5–29%) | W 2 chorobach |
| SKISKI proto-oncogene | Czasami (5–29%) | W 1 chorobie |
| SKIC3SKI3 subunit of superkiller complex | Czasami (5–29%) | W 1 chorobie |
| SLX4SLX4 structure-specific endonuclease subunit | Czasami (5–29%) | W 1 chorobie |
| SMAD4SMAD family member 4 | Czasami (5–29%) | W 1 chorobie |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Czasami (5–29%) | W 1 chorobie |
| SMARCA4SWI/SNF related BAF chromatin remodeling complex subunit ATPase 4 | Czasami (5–29%) | W 1 chorobie |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Czasami (5–29%) | W 1 chorobie |
| SMARCC2SWI/SNF related BAF chromatin remodeling complex subunit C2 | Czasami (5–29%) | W 1 chorobie |
| SMARCD1SWI/SNF related BAF chromatin remodeling complex subunit D1 | Czasami (5–29%) | W 1 chorobie |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Czasami (5–29%) | W 1 chorobie |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Czasami (5–29%) | W 1 chorobie |
| SMSspermine synthase | Czasami (5–29%) | W 1 chorobie |
| SOX11SRY-box transcription factor 11 | Czasami (5–29%) | W 1 chorobie |
| SOX2SRY-box transcription factor 2 | Czasami (5–29%) | W 2 chorobach |
| SOX4SRY-box transcription factor 4 | Czasami (5–29%) | W 1 chorobie |
| SPENspen family transcriptional repressor | Czasami (5–29%) | W 1 chorobie |
| SRCAPSnf2 related CREBBP activator protein | Czasami (5–29%) | W 2 chorobach |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Czasami (5–29%) | W 1 chorobie |
| TBX1T-box transcription factor 1 | Czasami (5–29%) | W 1 chorobie |
| TBX6T-box transcription factor 6 | Czasami (5–29%) | W 1 chorobie |
| TCF12transcription factor 12 | Czasami (5–29%) | W 1 chorobie |
| THOC6THO complex subunit 6 | Czasami (5–29%) | W 1 chorobie |
| TMEM94transmembrane protein 94 | Czasami (5–29%) | W 1 chorobie |
| TONSLtonsoku like, DNA repair protein | Czasami (5–29%) | W 1 chorobie |
| TRIM28tripartite motif containing 28 | Czasami (5–29%) | W 1 chorobie |
| TRIP13thyroid hormone receptor interactor 13 | Czasami (5–29%) | W 1 chorobie |
| TSR2TSR2 ribosome maturation factor | Czasami (5–29%) | W 1 chorobie |
| TUBBtubulin beta class I | Czasami (5–29%) | W 1 chorobie |
| UBE2Aubiquitin conjugating enzyme E2 A | Czasami (5–29%) | W 1 chorobie |
| UBE2Tubiquitin conjugating enzyme E2 T | Czasami (5–29%) | W 1 chorobie |
| UBE4Bubiquitination factor E4B | Czasami (5–29%) | W 1 chorobie |
| UBR1ubiquitin protein ligase E3 component n-recognin 1 | Czasami (5–29%) | W 2 chorobach |
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Czasami (5–29%) | W 1 chorobie |
| USP9Xubiquitin specific peptidase 9 X-linked | Czasami (5–29%) | W 1 chorobie |
| VPS35LVPS35 endosomal protein sorting factor like | Czasami (5–29%) | W 1 chorobie |
| WASHC5WASH complex subunit 5 | Czasami (5–29%) | W 2 chorobach |
| WNT5AWnt family member 5A | Czasami (5–29%) | W 1 chorobie |
| XRCC2X-ray repair cross complementing 2 | Czasami (5–29%) | W 1 chorobie |
| ZMPSTE24zinc metallopeptidase STE24 | Czasami (5–29%) | W 2 chorobach |
| ZMYM2zinc finger MYM-type containing 2 | Czasami (5–29%) | W 1 chorobie |
| ZNF699zinc finger protein 699 | Czasami (5–29%) | W 1 chorobie |
| ACBD6acyl-CoA binding domain containing 6 | Rzadko (1–4%) | W 1 chorobie |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Rzadko (1–4%) | W 1 chorobie |
| APC2APC regulator of Wnt signaling pathway 2 | Rzadko (1–4%) | W 1 chorobie |
| EHMT1euchromatic histone lysine methyltransferase 1 | Rzadko (1–4%) | W 1 chorobie |
| MTORmechanistic target of rapamycin kinase | Rzadko (1–4%) | W 1 chorobie |
| NKX2-1NK2 homeobox 1 | Rzadko (1–4%) | W 1 chorobie |
| NSD1nuclear receptor binding SET domain protein 1 | Rzadko (1–4%) | W 1 chorobie |
| SETBP1SET binding protein 1 | Rzadko (1–4%) | W 2 chorobach |
| SPTBN1spectrin beta, non-erythrocytic 1 | Rzadko (1–4%) | W 1 chorobie |
| SUCLG1succinate-CoA ligase GDP/ADP-forming subunit alpha | Rzadko (1–4%) | W 1 chorobie |
| ATRATR checkpoint kinase | Nie odnotowano | W 1 chorobie |
| ATRXATRX chromatin remodeler | Nie odnotowano | W 2 chorobach |
| BUB1BBUB1 mitotic checkpoint serine/threonine kinase B | Nie odnotowano | W 1 chorobie |
| CARS1cysteinyl-tRNA synthetase 1 | Nie odnotowano | W 1 chorobie |
| CDCA7cell division cycle associated 7 | Nie odnotowano | W 1 chorobie |
| CHRNGcholinergic receptor nicotinic gamma subunit | Nie odnotowano | W 1 chorobie |
| CUL4Bcullin 4B | Nie odnotowano | W 1 chorobie |
| CYP21A2cytochrome P450 family 21 subfamily A member 2 | Nie odnotowano | W 1 chorobie |
| DKC1dyskerin pseudouridine synthase 1 | Nie odnotowano | W 1 chorobie |
| FGFR1fibroblast growth factor receptor 1 | Nie odnotowano | W 2 chorobach |
| HUWE1HECT, UBA and WWE domain containing E3 ubiquitin protein ligase 1 | Nie odnotowano | W 1 chorobie |
| HYLS1HYLS1 centriolar and ciliogenesis associated | Nie odnotowano | W 1 chorobie |
| PCNTpericentrin | Nie odnotowano | W 1 chorobie |
| RBBP8RB binding protein 8, endonuclease | Nie odnotowano | W 1 chorobie |
| RLIMring finger protein, LIM domain interacting | Nie odnotowano | W 1 chorobie |
| RSPO1R-spondin 1 | Nie odnotowano | W 1 chorobie |
| SETD5SET domain containing 5 | Nie odnotowano | W 1 chorobie |
| SIX6SIX homeobox 6 | Nie odnotowano | W 1 chorobie |
| SSR4signal sequence receptor subunit 4 | Nie odnotowano | W 1 chorobie |
| STARsteroidogenic acute regulatory protein | Nie odnotowano | W 1 chorobie |
| TAPT1transmembrane anterior posterior transformation 1 | Nie odnotowano | W 1 chorobie |
| TFAP2Atranscription factor AP-2 alpha | Nie odnotowano | W 1 chorobie |
| TTC8tetratricopeptide repeat domain 8 | Nie odnotowano | W 1 chorobie |
| UBA1ubiquitin like modifier activating enzyme 1 | Nie odnotowano | W 1 chorobie |
| WDR35WD repeat domain 35 | Nie odnotowano | W 1 chorobie |
| WNT7AWnt family member 7A | Nie odnotowano | W 1 chorobie |
| ZMIZ1zinc finger MIZ-type containing 1 | Nie odnotowano | W 1 chorobie |
Jak często występuje wśród osób z jedną z chorób związanych z tym genem, najczęściej spośród wszystkich, według danych Human Phenotype Ontology. Te strony opisują cechy i badania, na których się opierają; nie są diagnozą, a w sprawie objawów należy zwrócić się do lekarza lub doradcy genetycznego.
Cechy podrzędne
Cechy nadrzędne
Skąd pochodzą te dane
- Human Phenotype Ontology, wydanie 2026-09-01: cecha, jej nazwy, definicja oraz geny z nią powiązane. Więcej informacji znajdą Państwo na stronie hpo.jax.org.
- Wydanie danych 2026.10.19-9814e911.
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