Trait
Wide nasal bridge
Increased breadth of the nasal bridge (and with it, the nasal root).
Summary
- Also called
- Broad flat nasal bridge, Broad nasal bridge, Broad nasal root, Broadened nasal bridge, Increased breadth of bridge of nose, Increased breadth of nasal bridge, Increased width of bridge of nose, Increased width of nasal bridge, Nasal bridge broad, Wide bridge of nose, Widened nasal bridge, Nasal bridge, wide
- Body system
- Abnormality of head or neck
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
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Get my Genome Test215 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.
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- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 13 of these genesPEX10PEX12PEX14PEX19PEX1PEX11BAbout this report →
- GPI Anchor Biosynthesis DefectsReads 11 of these genesPGAP2PGAP3PIGLPIGOPIGWPIGGAbout this report →
Show 211 more reports
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- Lissencephaly Spectrum DisordersReads 11 of these genesAPC2NDE1ACTBACTG1RAB18RAB3GAP1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 12 of these genesERCC1ERCC2ERCC5RAB18RAB3GAP1RAB3GAP2About this report →
- Waardenburg SyndromeReads 6 of these genesPAX3EDN3EDNRBMITFSOX10SNAI2About this report →
- Epilepsy (Full Panel)Reads 28 of these genesFLNARNU2-2SLC35A2STRADAATP6V1B2CPLX1About this report →
- Treacher Collins SyndromeReads 4 of these genesPOLR1BPOLR1CPOLR1DTCOF1About this report →
- Syndromic CraniosynostosisReads 9 of these genesFGFR1IFT122IFT52WDR19SKIERFAbout this report →
- Fraser SyndromeReads 3 of these genesFRAS1FREM2GRIP1About this report →
- Noonan SyndromeReads 8 of these genesBRAFERFPTPN11RAF1KRASLZTR1About this report →
- Other Inherited LeukodystrophiesReads 15 of these genesPEX10PEX12PEX14PEX19PEX1PEX11BAbout this report →
- Inherited Neurodegenerative DisordersReads 30 of these genesFLVCR1NALCNPEX10PEX12PEX14PEX19About this report →
- Ellis-van Creveld Syndrome and Cranioectodermal DysplasiaReads 4 of these genesIFT122IFT52WDR19WDR35About this report →
- Cutis LaxaReads 6 of these genesLTBP1LTBP4RIN2ELNATP6V1AATP6V0A2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 22 of these genesDHX9PEX10PEX12PEX14PEX19SCO2About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 2 of these genesPIK3CDPIK3R1About this report →
- Cantú SyndromeReads 2 of these genesABCC9KCNJ8About this report →
- DOORS SyndromeReads 2 of these genesATP6V1B2TBC1D24About this report →
- Kabuki SyndromeReads 2 of these genesKDM6AKMT2DAbout this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 2 of these genesPTCH1SUFUAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 6 of these genesMYT1LSETD5PAN2TBCKZMYM2RNU4-2About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 5 of these genesADAMTS3CCBE1FAT4KIF11SOX18About this report →
- Familial Periodic ParalysisReads 2 of these genesKCNJ2SCN4AAbout this report →
- Immuno-Osseous DysplasiasReads 2 of these genesSMARCAL1RMRPAbout this report →
- Joubert Syndrome And Related DisordersReads 7 of these genesKIF7OFD1MKS1SUFUTOGARAM1ARMC9About this report →
- Inherited ThrombocytopeniasReads 6 of these genesACTBGNEGP1BBCDC42FLI1GATA1About this report →
- Other Inborn Errors of ImmunityReads 15 of these genesAP3B1HYOU1LIG4SKIC2SMARCAL1NCF1About this report →
- Hypertrophic CardiomyopathyReads 8 of these genesBRAFERFPTPN11RAF1KRASLZTR1About this report →
- Complex Neurodevelopmental Disorder (TRRAP, MYH10, RERE, SOX11)Reads 2 of these genesRERETRRAPAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 2 of these genesPDE4DPRKAR1AAbout this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- Aarskog-Scott SyndromeReads 1 of these genesFGD1About this report →
- Acromelic Frontonasal DysostosisReads 1 of these genesZSWIM6About this report →
- Aminoacylase 1 DeficiencyReads 1 of these genesACY1About this report →
- Amyotrophic Lateral Sclerosis Susceptibility 24 (NEK1)Reads 1 of these genesNEK1About this report →
- Au-Kline SyndromeReads 1 of these genesHNRNPKAbout this report →
- Burn-McKeown SyndromeReads 1 of these genesTXNL4AAbout this report →
- Cardiac-Urogenital SyndromeReads 1 of these genesMYRFAbout this report →
- Craniofrontonasal SyndromeReads 1 of these genesEFNB1About this report →
- CTNNB1 SyndromeReads 1 of these genesCTNNB1About this report →
- Deficiency of Adenosine Deaminase 2 (DADA2)Reads 1 of these genesADA2About this report →
- DeSanto-Shinawi SyndromeReads 1 of these genesWACAbout this report →
- Dias-Logan SyndromeReads 1 of these genesBCL11AAbout this report →
- Dravet SyndromeReads 1 of these genesSCN1AAbout this report →
- Dyssegmental Dysplasia, Silverman-Handmaker TypeReads 1 of these genesHSPG2About this report →
- EBF3-Related Neurodevelopmental Disorder (HADDS)Reads 1 of these genesEBF3About this report →
- Elsahy-Waters SyndromeReads 1 of these genesCDH11About this report →
- FAT4-Related Neurodevelopmental DisorderReads 1 of these genesFAT4About this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- Floating-Harbor SyndromeReads 1 of these genesSRCAPAbout this report →
- Frank-Ter Haar SyndromeReads 1 of these genesSH3PXD2BAbout this report →
- Frontonasal Dysplasia 3 (ALX1)Reads 1 of these genesALX1About this report →
- Frontonasal Dysplasia with Alopecia and Genital Anomaly (ALX4)Reads 1 of these genesALX4About this report →
- FrontorhinyReads 1 of these genesALX3About this report →
- Greig Cephalopolysyndactyly SyndromeReads 1 of these genesGLI3About this report →
- Hajdu-Cheney SyndromeReads 1 of these genesNOTCH2About this report →
- Hereditary RetinoblastomaReads 1 of these genesRB1About this report →
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
- JARID2-Related Neurodevelopmental DisorderReads 1 of these genesJARID2About this report →
- KAT6B-Related DisordersReads 1 of these genesKAT6BAbout this report →
- KCNH1-Related DisorderReads 1 of these genesKCNH1About this report →
- KDM1A-Related Neurodevelopmental DisorderReads 1 of these genesKDM1AAbout this report →
- Keutel SyndromeReads 1 of these genesMGPAbout this report →
- Labyrinthine Aplasia, Microtia and Microdontia (LAMM)Reads 1 of these genesFGF3About this report →
- Lamb-Shaffer SyndromeReads 1 of these genesSOX5About this report →
- Lessel-Kreienkamp SyndromeReads 1 of these genesAGO2About this report →
- Microcephalic Osteodysplastic Primordial Dwarfism Type IIReads 1 of these genesPCNTAbout this report →
- Microcephaly and Chorioretinopathy 1 (TUBGCP6)Reads 1 of these genesTUBGCP6About this report →
- Mitchell SyndromeReads 1 of these genesACOX1About this report →
- Mowat-Wilson SyndromeReads 1 of these genesZEB2About this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- Mucopolysaccharidosis-Plus SyndromeReads 1 of these genesVPS33AAbout this report →
- Mulibrey NanismReads 1 of these genesTRIM37About this report →
- NDE1-Related MicrolissencephalyReads 1 of these genesNDE1About this report →
- NOG-Related Symphalangism Spectrum DisorderReads 1 of these genesNOGAbout this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- Otofaciocervical Syndrome Type 2 (PAX1)Reads 1 of these genesPAX1About this report →
- PBX1-Related Kidney and Urinary Tract AnomaliesReads 1 of these genesPBX1About this report →
- Perlman SyndromeReads 1 of these genesDIS3L2About this report →
- Phenylketonuria (PKU)Reads 1 of these genesPAHAbout this report →
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- POLR1C-Related DisorderReads 1 of these genesPOLR1CAbout this report →
- PPP1R21-Related Neurodevelopmental DisorderReads 1 of these genesPPP1R21About this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- Primary Microcephaly 26 (LMNB1)Reads 1 of these genesLMNB1About this report →
- Radio-Tartaglia SyndromeReads 1 of these genesSPENAbout 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 →
- Sandestig-Stefanova SyndromeReads 1 of these genesNUP188About this report →
- Schwartz-Jampel Syndrome Type 1Reads 1 of these genesHSPG2About this report →
- SCN4A-Related Congenital MyopathyReads 1 of these genesSCN4AAbout this report →
- Short-Rib Thoracic Dysplasia 7 (WDR35)Reads 1 of these genesWDR35About this report →
- SHOX Deficiency (Leri-Weill and Langer Dysplasia)Reads 1 of these genesSHOXAbout this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- Smith-Lemli-Opitz SyndromeReads 1 of these genesDHCR7About this report →
- Snijders Blok-Campeau SyndromeReads 1 of these genesCHD3About this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
- Stankiewicz-Isidor SyndromeReads 1 of these genesPSMD12About this report →
- TARP SyndromeReads 1 of these genesRBM10About this report →
- TMEM94-Related Intellectual Disability with Heart DefectsReads 1 of these genesTMEM94About this report →
- TRAPPC9-Related Intellectual DisabilityReads 1 of these genesTRAPPC9About this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- Wiedemann-Steiner SyndromeReads 1 of these genesKMT2AAbout this report →
- X-Linked Opitz G/BBB SyndromeReads 1 of these genesMID1About this report →
- ZTTK SyndromeReads 1 of these genesSONAbout this report →
- DNA Repair DiseaseReads 6 of these genesNBNERCC1ERCC2ERCC5ERCC6FANCLAbout this report →
- Hereditary Methaemoglobinaemia and Unstable HaemoglobinsReads 2 of these genesHBA1HBA2About this report →
- ThalassaemiaReads 2 of these genesHBA1HBA2About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 5 of these genesTOR1AACTBSCN4AWARS2SLC2A1About this report →
- Inherited Congenital Heart DefectsReads 3 of these genesFLNAELNGATA4About this report →
- Peroxisomal Enzyme Disorders & Refsum DiseaseReads 2 of these genesACOX1GNPATAbout this report →
- Lysosomal Storage DiseaseReads 6 of these genesIDUAAGAGNENEU1ARSKCTSDAbout this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 2 of these genesAGANEU1About this report →
- Congenital Cranial Dysinnervation DisordersReads 2 of these genesCHN1MAFBAbout this report →
- Ectodermal DysplasiasReads 3 of these genesNECTIN1KREMEN1TP63About this report →
- PolycythemiaReads 2 of these genesHBA1HBA2About this report →
- Alagille SyndromeReads 1 of these genesNOTCH2About this report →
- Cleidocranial DysplasiaReads 1 of these genesRUNX2About this report →
- Enlarged Parietal Foramina (MSX2)Reads 1 of these genesALX4About this report →
- FLNB-Related Skeletal Dysplasia (Larsen Spectrum)Reads 1 of these genesFLNBAbout this report →
- Hereditary FibromatosesReads 1 of these genesPDGFRBAbout this report →
- Hereditary Multiple OsteochondromasReads 1 of these genesEXT1About this report →
- Inherited ArthropathiesReads 1 of these genesANKHAbout this report →
- Malignant Hyperthermia SusceptibilityReads 1 of these genesRYR1About this report →
- Müllerian Aplasia (MRKH Syndrome)Reads 1 of these genesTBX6About this report →
- Rare Inherited Megaloblastic AnaemiasReads 1 of these genesUMPSAbout this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- Charcot-Marie-Tooth DiseaseReads 6 of these genesDHX9SCO2LMNASLC12A6YARS1MPV17About this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 2 of these genesFOXC1PITX2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 5 of these genesFLVCR1PEX6MKS1SNX14AHI1About this report →
- Marfan Like SyndromesReads 2 of these genesSKIFBN1About this report →
- Meckel SyndromeReads 2 of these genesKIF14MKS1About this report →
- Primary Mitochondrial DiseaseReads 7 of these genesSCO2DNAJC30NDUFB11FBXL4LRPPRCMPV17About this report →
- Congenital Myasthenic SyndromeReads 3 of these genesRAPSNALG2SCN4AAbout this report →
- Familial Hemiplegic MigraineReads 1 of these genesSCN1AAbout this report →
- Hirschsprung Disease & Related Enteric NeurocristopathiesReads 1 of these genesKIFBPAbout this report →
- Leukocyte Adhesion DeficiencyReads 1 of these genesSLC35C1About this report →
- MedulloblastomaReads 1 of these genesSUFUAbout this report →
- Monogenic Precocious PubertyReads 1 of these genesDLK1About this report →
- Dilated CardiomyopathyReads 4 of these genesLMNAPRDM16ABCC9RAF1About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 2 of these genesAPC2CAMSAP1About this report →
- Osteogenesis ImperfectaReads 3 of these genesSP7ATP6V0A2TENT5AAbout this report →
- Rare Monogenic Autoinflammatory DiseasesReads 3 of these genesSKIC2SKIC3ADA2About this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesLMNB1About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPRKAR1AAbout this report →
- Familial Atrial FibrillationReads 1 of these genesKCNJ2About this report →
- Hereditary Gastrointestinal Stromal TumourReads 1 of these genesKITAbout this report →
- MelanomaReads 1 of these genesMITFAbout this report →
- Multiple Synostoses Syndrome (FGF9)Reads 1 of these genesNOGAbout this report →
- NeurofibromatosisReads 1 of these genesLZTR1About this report →
- Short Qt SyndromeReads 1 of these genesKCNJ2About this report →
- Hereditary Spastic ParaplegiaReads 4 of these genesWASHC5AP4B1AP4E1AP4S1About this report →
- Leigh SyndromeReads 4 of these genesSCO2FBXL4LRPPRCPDHA1About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 2 of these genesGATA4ATRXAbout this report →
- Congenital MyopathiesReads 2 of these genesTPM2RYR1About this report →
- PancreatitisReads 1 of these genesTRPV6About this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesSOSTAbout this report →
- Autoimmune DiseaseReads 2 of these genesSTAT3KRASAbout this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 2 of these genesCLP1TOE1About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- Cornelia de Lange SyndromeReads 1 of these genesRAD21About this report →
- Growth Hormone Insensitivity & IGF-1 Axis DisordersReads 1 of these genesIGF1RAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 2 of these genesGLI3PTCH1About this report →
- VitreoretinopathyReads 2 of these genesCOL11A1CTNNB1About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Basal Ganglia CalcificationReads 1 of these genesPDGFRBAbout this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT3About this report →
- Severe Combined ImmunodeficiencyReads 2 of these genesLIG4PRKDCAbout this report →
- Disorders of Glycine & Serine MetabolismReads 1 of these genesSLC1A4About this report →
- GlaucomaReads 1 of these genesFOXC1About this report →
- Hereditary Rickets (Hypophosphatemic and Vitamin D-Dependent)Reads 1 of these genesVDRAbout this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 2 of these genesSNAP29GJA1About this report →
- Retinitis PigmentosaReads 3 of these genesFLVCR1IFT140OFD1About this report →
- Autism Spectrum DisorderReads 1 of these genesCHD8About this report →
- Inherited Platelet Function DisordersReads 1 of these genesGP1BBAbout this report →
- Pyruvate Dehydrogenase & Pyruvate Carboxylase DeficiencyReads 1 of these genesPDHA1About this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 1 of these genesPIK3R1About this report →
- Long QT SyndromeReads 1 of these genesKCNJ2About this report →
- Hearing Loss and DeafnessReads 3 of these genesACTG1COL11A1TBC1D24About this report →
- Familial HypomagnesemiaReads 1 of these genesTRPV6About this report →
- Hermansky-Pudlak SyndromeReads 1 of these genesAP3B1About this report →
- Polycystic Kidney DiseaseReads 1 of these genesIFT140About this report →
- Coffin-Siris SyndromeReads 1 of these genesARID1BAbout this report →
- LipodystrophyReads 1 of these genesLMNAAbout this report →
- Severe Congenital NeutropeniaReads 1 of these genesG6PC3About this report →
- Hypogonadotropic HypogonadismReads 2 of these genesFGFR1RAB3GAP2About this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- Myofibrillar MyopathiesReads 1 of these genesRYR1About this report →
- Female InfertilityReads 2 of these genesFOXL2TP63About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesCTSDAbout this report →
- OsteopetrosisReads 1 of these genesAMER1About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesKCNJ5About this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesKIF14About this report →
- Fanconi AnemiaReads 1 of these genesFANCLAbout this report →
- Distal MyopathiesReads 1 of these genesGNEAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- Neonatal Diabetes MellitusReads 1 of these genesGATA4About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesWDR19About this report →
- Ehlers-Danlos SyndromeReads 1 of these genesB4GALT7About this report →
- Bardet-Biedl and Alström SyndromesReads 1 of these genesMKS1About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesMAFAbout this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesPOLR1CAbout this report →
- Diabetes MellitusReads 1 of these genesGATA4About this report →
- Thyroid CancerReads 1 of these genesTRPV6About 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 →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Primary Ciliary DyskinesiaReads 1 of these genesCENPFAbout this report →
Read the genes linked to Wide nasal bridge, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test538 genes linked to Wide nasal bridge
Changes in these genes cause rare conditions in which Wide nasal bridge is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| AGO1argonaute RISC component 1 | Always | In 1 condition |
| ALX1ALX homeobox 1 | Always | In 2 conditions |
| ALX3ALX homeobox 3 | Always | In 1 condition |
| ALX4ALX homeobox 4 | Always | In 1 condition |
| ANKHANKH inorganic pyrophosphate transport regulator | Always | In 2 conditions |
| AP3B1adaptor related protein complex 3 subunit beta 1 | Always | In 1 condition |
| APC2APC regulator of Wnt signaling pathway 2 | Always | In 1 condition |
| CAMSAP1calmodulin regulated spectrin associated protein 1 | Always | In 1 condition |
| CDH11cadherin 11 | Always | In 1 condition |
| CHD8chromodomain helicase DNA binding protein 8 | Always | In 2 conditions |
| CILK1ciliogenesis associated kinase 1 | Always | In 2 conditions |
| CLP1cleavage factor polyribonucleotide kinase subunit 1 | Always | In 2 conditions |
| CREBBPCREB binding lysine acetyltransferase | Always | In 1 condition |
| CRNKL1crooked neck pre-mRNA splicing factor 1 | Always | In 1 condition |
| DHX9DExH-box helicase 9 | Always | In 1 condition |
| DIS3L2DIS3 like 3'-5' exoribonuclease 2 | Always | In 2 conditions |
| DMRT2doublesex and mab-3 related transcription factor 2 | Always | In 1 condition |
| DRG1developmentally regulated GTP binding protein 1 | Always | In 1 condition |
| DVL1dishevelled segment polarity protein 1 | Always | In 3 conditions |
| DVL3dishevelled segment polarity protein 3 | Always | In 2 conditions |
| EIF4A2eukaryotic translation initiation factor 4A2 | Always | In 1 condition |
| EP300EP300 lysine acetyltransferase | Always | In 1 condition |
| ERI1exoribonuclease 1 | Always | In 1 condition |
| ESAMendothelial cell adhesion molecule | Always | In 1 condition |
| FBXO31F-box protein 31 | Always | In 1 condition |
| FGD1FYVE, RhoGEF and PH domain containing 1 | Always | In 2 conditions |
| FGFR1fibroblast growth factor receptor 1 | Always | In 2 conditions |
| FILIP1filamin A interacting protein 1 | Always | In 1 condition |
| FLNAfilamin A | Always | In 5 conditions |
| FLVCR1FLVCR choline and heme transporter 1 | Always | In 1 condition |
| GPC3glypican 3 | Always | In 2 conditions |
| HYAL2hyaluronidase 2 | Always | In 1 condition |
| HYOU1hypoxia up-regulated 1 | Always | In 1 condition |
| IDUAalpha-L-iduronidase | Always | In 2 conditions |
| IFT122intraflagellar transport 122 | Always | In 1 condition |
| IFT140intraflagellar transport 140 | Always | In 2 conditions |
| IFT52intraflagellar transport 52 | Always | In 1 condition |
| IRX5iroquois homeobox 5 | Always | In 1 condition |
| JKAMPJNK1/MAPK8 associated membrane protein | Always | In 1 condition |
| KDM1Alysine demethylase 1A | Always | In 2 conditions |
Show 498 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| KIAA0753KIAA0753 | Always | In 2 conditions |
| KIF7kinesin family member 7 | Always | In 3 conditions |
| LIG4DNA ligase 4 | Always | In 2 conditions |
| LRRC7leucine rich repeat containing 7 | Always | In 1 condition |
| LTBP1latent transforming growth factor beta binding protein 1 | Always | In 1 condition |
| LTBP4latent transforming growth factor beta binding protein 4 | Always | In 1 condition |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Always | In 3 conditions |
| MAPRE2microtubule associated protein RP/EB family member 2 | Always | In 1 condition |
| MDGA2MAM domain containing glycosylphosphatidylinositol anchor 2 | Always | In 1 condition |
| MED12mediator complex subunit 12 | Always | In 1 condition |
| MGPmatrix Gla protein | Always | In 1 condition |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Always | In 2 conditions |
| MYH3myosin heavy chain 3 | Always | In 3 conditions |
| MYT1Lmyelin transcription factor 1 like | Always | In 1 condition |
| NALCNsodium leak channel, non-selective | Always | In 4 conditions |
| NAV3neuron navigator 3 | Always | In 1 condition |
| NBNnibrin | Always | In 1 condition |
| NDE1nudE neurodevelopment protein 1 | Always | In 2 conditions |
| NFASCneurofascin | Always | In 1 condition |
| NUDT2nudix hydrolase 2 | Always | In 1 condition |
| NUP188nucleoporin 188 | Always | In 1 condition |
| NUP88nucleoporin 88 | Always | In 1 condition |
| OFD1OFD1 centriole and centriolar satellite protein | Always | In 3 conditions |
| PAX3paired box 3 | Always | In 3 conditions |
| PDGFRBplatelet derived growth factor receptor beta | Always | In 1 condition |
| PEX10peroxisomal biogenesis factor 10 | Always | In 3 conditions |
| PEX12peroxisomal biogenesis factor 12 | Always | In 3 conditions |
| PEX14peroxisomal biogenesis factor 14 | Always | In 3 conditions |
| PEX19peroxisomal biogenesis factor 19 | Always | In 3 conditions |
| PGAP2post-GPI attachment to proteins 2 | Always | In 2 conditions |
| PGAP3post-GPI attachment to proteins phospholipase 3 | Always | In 2 conditions |
| PIGLphosphatidylinositol glycan anchor biosynthesis class L | Always | In 2 conditions |
| PIGOphosphatidylinositol glycan anchor biosynthesis class O | Always | In 2 conditions |
| PIGWphosphatidylinositol glycan anchor biosynthesis class W | Always | In 2 conditions |
| PPFIA3PPFI scaffold protein A3 | Always | In 1 condition |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Always | In 2 conditions |
| RAC3Rac family small GTPase 3 | Always | In 1 condition |
| RAD21RAD21 cohesin complex component | Always | In 2 conditions |
| RAPSNreceptor associated protein of the synapse | Always | In 1 condition |
| RBL2RB transcriptional corepressor like 2 | Always | In 1 condition |
| RIN2Ras and Rab interactor 2 | Always | In 1 condition |
| RNU2-2RNA, U2 small nuclear 2 | Always | In 1 condition |
| RSRC1arginine and serine rich coiled-coil 1 | Always | In 1 condition |
| SCNM1sodium channel modifier 1 | Always | In 1 condition |
| SCO2synthesis of cytochrome C oxidase 2 | Always | In 1 condition |
| SEC23ASEC23 homolog A, COPII component | Always | In 1 condition |
| SETD5SET domain containing 5 | Always | In 1 condition |
| SIN3ASIN3 transcription regulator family member A | Always | In 1 condition |
| SKIC2SKI2 subunit of superkiller complex | Always | In 2 conditions |
| SLC35A2solute carrier family 35 member A2 | Always | In 1 condition |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Always | In 1 condition |
| SNAP29synaptosome associated protein 29 | Always | In 1 condition |
| SPOUT1SPOUT domain containing methyltransferase 1 | Always | In 1 condition |
| SRD5A3steroid 5 alpha-reductase 3 | Always | In 1 condition |
| STRADASTE20 related adaptor alpha | Always | In 1 condition |
| TAF4TATA-box binding protein associated factor 4 | Always | In 1 condition |
| TASP1taspase 1 | Always | In 1 condition |
| TMCO1transmembrane and coiled-coil domains 1 | Always | In 1 condition |
| TOR1Atorsin family 1 member A | Always | In 1 condition |
| UBAP2Lubiquitin associated protein 2 like | Always | In 1 condition |
| UGGT1UDP-glucose glycoprotein glucosyltransferase 1 | Always | In 1 condition |
| UNC13Aunc-13 homolog A | Always | In 1 condition |
| VDRvitamin D receptor | Always | In 1 condition |
| WDR19WD repeat domain 19 | Always | In 1 condition |
| ZSWIM6zinc finger SWIM-type containing 6 | Always | In 1 condition |
| ACTBactin beta | Very often (80–99%) | In 3 conditions |
| ACTG1actin gamma 1 | Very often (80–99%) | In 1 condition |
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Very often (80–99%) | In 1 condition |
| ADAMTSL2ADAMTS like 2 | Very often (80–99%) | In 1 condition |
| AGAaspartylglucosaminidase | Very often (80–99%) | In 1 condition |
| ARVCFARVCF delta catenin family member | Very often (80–99%) | In 1 condition |
| ATP6V1B2ATPase H+ transporting V1 subunit B2 | Very often (80–99%) | In 1 condition |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Very often (80–99%) | In 1 condition |
| BCL11ABCL11 transcription factor A | Very often (80–99%) | In 1 condition |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Very often (80–99%) | In 1 condition |
| CASZ1castor zinc finger 1 | Very often (80–99%) | In 1 condition |
| CCBE1collagen and calcium binding EGF domains 1 | Very often (80–99%) | In 2 conditions |
| CCDC22CCC complex scaffolding subunit CCDC22 | Very often (80–99%) | In 1 condition |
| CKAP2Lcytoskeleton associated protein 2L | Very often (80–99%) | In 2 conditions |
| CLIP2CAP-Gly domain containing linker protein 2 | Very often (80–99%) | In 1 condition |
| COL11A1collagen type XI alpha 1 chain | Very often (80–99%) | In 1 condition |
| COMTcatechol-O-methyltransferase | Very often (80–99%) | In 1 condition |
| CPLX1complexin 1 | Very often (80–99%) | In 2 conditions |
| CTBP1C-terminal binding protein 1 | Very often (80–99%) | In 2 conditions |
| CTNND2catenin delta 2 | Very often (80–99%) | In 1 condition |
| DHCR77-dehydrocholesterol reductase | Very often (80–99%) | In 2 conditions |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Very often (80–99%) | In 1 condition |
| DPYSL5dihydropyrimidinase like 5 | Very often (80–99%) | In 2 conditions |
| EFNB1ephrin B1 | Very often (80–99%) | In 2 conditions |
| EIF4Heukaryotic translation initiation factor 4H | Very often (80–99%) | In 1 condition |
| ELNelastin | Very often (80–99%) | In 1 condition |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Very often (80–99%) | In 1 condition |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Very often (80–99%) | In 1 condition |
| ERCC5ERCC excision repair 5, endonuclease | Very often (80–99%) | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Very often (80–99%) | In 1 condition |
| FAT4FAT atypical cadherin 4 | Very often (80–99%) | In 3 conditions |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Very often (80–99%) | In 1 condition |
| FZD2frizzled class receptor 2 | Very often (80–99%) | In 2 conditions |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Very often (80–99%) | In 1 condition |
| GJA1gap junction protein alpha 1 | Very often (80–99%) | In 2 conditions |
| GNEglucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase | Very often (80–99%) | In 2 conditions |
| GP1BBglycoprotein Ib platelet subunit beta | Very often (80–99%) | In 1 condition |
| GTF2Igeneral transcription factor IIi | Very often (80–99%) | In 1 condition |
| GTF2IRD1GTF2I repeat domain containing 1 | Very often (80–99%) | In 1 condition |
| GTF2IRD2GTF2I repeat domain containing 2 | Very often (80–99%) | In 1 condition |
| HIRAhistone cell cycle regulator | Very often (80–99%) | In 1 condition |
| HSPG2heparan sulfate proteoglycan 2 | Very often (80–99%) | In 3 conditions |
| INTS1integrator complex subunit 1 | Very often (80–99%) | In 1 condition |
| JMJD1Cjumonji domain containing 1C | Very often (80–99%) | In 1 condition |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Very often (80–99%) | In 1 condition |
| KCNMA1potassium calcium-activated channel subfamily M alpha 1 | Very often (80–99%) | In 1 condition |
| KDM6Alysine demethylase 6A | Very often (80–99%) | In 1 condition |
| KMT2Alysine methyltransferase 2A | Very often (80–99%) | In 2 conditions |
| KMT2Dlysine methyltransferase 2D | Very often (80–99%) | In 2 conditions |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Very often (80–99%) | In 2 conditions |
| LIMK1LIM domain kinase 1 | Very often (80–99%) | In 1 condition |
| LMNAlamin A/C | Very often (80–99%) | In 1 condition |
| LUZP1leucine zipper protein 1 | Very often (80–99%) | In 1 condition |
| METTL27methyltransferase like 27 | Very often (80–99%) | In 1 condition |
| MID1midline 1 | Very often (80–99%) | In 2 conditions |
| MMP23Bmatrix metallopeptidase 23B | Very often (80–99%) | In 1 condition |
| NCF1neutrophil cytosolic factor 1 | Very often (80–99%) | In 1 condition |
| NELFAnegative elongation factor complex member A | Very often (80–99%) | In 1 condition |
| NEU1neuraminidase 1 | Very often (80–99%) | In 1 condition |
| NSD2nuclear receptor binding SET domain protein 2 | Very often (80–99%) | In 3 conditions |
| NXNnucleoredoxin | Very often (80–99%) | In 2 conditions |
| PDE4Dphosphodiesterase 4D | Very often (80–99%) | In 1 condition |
| PDPNpodoplanin | Very often (80–99%) | In 1 condition |
| PEX1peroxisomal biogenesis factor 1 | Very often (80–99%) | In 3 conditions |
| PEX11Bperoxisomal biogenesis factor 11 beta | Very often (80–99%) | In 2 conditions |
| PEX13peroxisomal biogenesis factor 13 | Very often (80–99%) | In 2 conditions |
| PEX16peroxisomal biogenesis factor 16 | Very often (80–99%) | In 2 conditions |
| PEX2peroxisomal biogenesis factor 2 | Very often (80–99%) | In 2 conditions |
| PEX26peroxisomal biogenesis factor 26 | Very often (80–99%) | In 2 conditions |
| PEX3peroxisomal biogenesis factor 3 | Very often (80–99%) | In 2 conditions |
| PEX5peroxisomal biogenesis factor 5 | Very often (80–99%) | In 3 conditions |
| PEX6peroxisomal biogenesis factor 6 | Very often (80–99%) | In 2 conditions |
| PIGGphosphatidylinositol glycan anchor biosynthesis class G (EMM blood group) | Very often (80–99%) | In 1 condition |
| PIGNphosphatidylinositol glycan anchor biosynthesis class N | Very often (80–99%) | In 1 condition |
| PIGVphosphatidylinositol glycan anchor biosynthesis class V | Very often (80–99%) | In 2 conditions |
| PQBP1polyglutamine binding protein 1 | Very often (80–99%) | In 2 conditions |
| PRDM16PR/SET domain 16 | Very often (80–99%) | In 1 condition |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Very often (80–99%) | In 1 condition |
| PRKCZprotein kinase C zeta | Very often (80–99%) | In 1 condition |
| PTH1Rparathyroid hormone 1 receptor | Very often (80–99%) | In 1 condition |
| RAB18RAB18, member RAS oncogene family | Very often (80–99%) | In 1 condition |
| RAB3GAP1RAB3 GTPase activating protein catalytic subunit 1 | Very often (80–99%) | In 2 conditions |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Very often (80–99%) | In 1 condition |
| RAI1retinoic acid induced 1 | Very often (80–99%) | In 2 conditions |
| RB1RB transcriptional corepressor 1 | Very often (80–99%) | In 1 condition |
| RELREL proto-oncogene, NF-kB subunit | Very often (80–99%) | In 1 condition |
| REREarginine-glutamic acid dipeptide repeats | Very often (80–99%) | In 1 condition |
| RFC2replication factor C subunit 2 | Very often (80–99%) | In 1 condition |
| ROR2ROR family WNT receptor 2 | Very often (80–99%) | In 2 conditions |
| RREB1ras responsive element binding protein 1 | Very often (80–99%) | In 1 condition |
| SEC24CSEC24 homolog C, COPII component | Very often (80–99%) | In 1 condition |
| SEMA5Asemaphorin 5A | Very often (80–99%) | In 1 condition |
| SH3PXD2BSH3 and PX domains 2B | Very often (80–99%) | In 1 condition |
| SHOXSHOX homeobox | Very often (80–99%) | In 1 condition |
| SKISKI proto-oncogene | Very often (80–99%) | In 1 condition |
| SOSTsclerostin | Very often (80–99%) | In 3 conditions |
| SP7Sp7 transcription factor | Very often (80–99%) | In 1 condition |
| SPENspen family transcriptional repressor | Very often (80–99%) | In 2 conditions |
| STX1Asyntaxin 1A | Very often (80–99%) | In 1 condition |
| TBC1D20TBC1 domain family member 20 | Very often (80–99%) | In 1 condition |
| TBC1D24TBC1 domain family member 24 | Very often (80–99%) | In 2 conditions |
| TBC1D7TBC1 domain family member 7 | Very often (80–99%) | In 1 condition |
| TBL2transducin beta like 2 | Very often (80–99%) | In 1 condition |
| TBX1T-box transcription factor 1 | Very often (80–99%) | In 1 condition |
| TMEM270transmembrane protein 270 | Very often (80–99%) | In 1 condition |
| TRAPPC9trafficking protein particle complex subunit 9 | Very often (80–99%) | In 2 conditions |
| TWIST2twist family bHLH transcription factor 2 | Very often (80–99%) | In 2 conditions |
| UBE4Bubiquitination factor E4B | Very often (80–99%) | In 1 condition |
| UFD1ubiquitin recognition factor in ER associated degradation 1 | Very often (80–99%) | In 1 condition |
| VPS35LVPS35 endosomal protein sorting factor like | Very often (80–99%) | In 1 condition |
| VPS37DVPS37D subunit of ESCRT-I | Very often (80–99%) | In 1 condition |
| WASHC5WASH complex subunit 5 | Very often (80–99%) | In 1 condition |
| WNT5AWnt family member 5A | Very often (80–99%) | In 2 conditions |
| XPO1exportin 1 | Very often (80–99%) | In 1 condition |
| ABCC9ATP binding cassette subfamily C member 9 | Often (30–79%) | In 2 conditions |
| ADAMTSL1ADAMTS like 1 | Often (30–79%) | In 1 condition |
| ADNPactivity dependent neuroprotector homeobox | Often (30–79%) | In 1 condition |
| ALG2ALG2 alpha-1,3/1,6-mannosyltransferase | Often (30–79%) | In 2 conditions |
| AMER1APC membrane recruitment protein 1 | Often (30–79%) | In 2 conditions |
| ARID1BAT-rich interaction domain 1B | Often (30–79%) | In 1 condition |
| ARSKarylsulfatase family member K | Often (30–79%) | In 1 condition |
| ASXL1ASXL transcriptional regulator 1 | Often (30–79%) | In 2 conditions |
| ASXL3ASXL transcriptional regulator 3 | Often (30–79%) | In 1 condition |
| ATP6V1AATPase H+ transporting V1 subunit A | Often (30–79%) | In 1 condition |
| AUTS2activator of transcription and developmental regulator AUTS2 | Often (30–79%) | In 2 conditions |
| B4GALT1beta-1,4-galactosyltransferase 1 | Often (30–79%) | In 1 condition |
| B4GALT7beta-1,4-galactosyltransferase 7 | Often (30–79%) | In 2 conditions |
| BPTFbromodomain PHD finger transcription factor | Often (30–79%) | In 1 condition |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Often (30–79%) | In 1 condition |
| C1GALT1C1C1GALT1 specific chaperone 1 | Often (30–79%) | In 1 condition |
| CASKcalcium/calmodulin dependent serine protein kinase | Often (30–79%) | In 3 conditions |
| CCNQcyclin Q | Often (30–79%) | In 1 condition |
| CDK10cyclin dependent kinase 10 | Often (30–79%) | In 1 condition |
| COG1component of oligomeric golgi complex 1 | Often (30–79%) | In 2 conditions |
| COX7Bcytochrome c oxidase subunit 7B | Often (30–79%) | In 1 condition |
| CTNNB1catenin beta 1 | Often (30–79%) | In 1 condition |
| DOT1LDOT1 like histone lysine methyltransferase | Often (30–79%) | In 1 condition |
| DPH5diphthamide biosynthesis 5 | Often (30–79%) | In 1 condition |
| EBF3EBF transcription factor 3 | Often (30–79%) | In 1 condition |
| EDN3endothelin 3 | Often (30–79%) | In 1 condition |
| EDNRBendothelin receptor type B | Often (30–79%) | In 1 condition |
| ERFETS2 repressor factor | Often (30–79%) | In 1 condition |
| EXOC2exocyst complex component 2 | Often (30–79%) | In 1 condition |
| FBN1fibrillin 1 | Often (30–79%) | In 1 condition |
| FGF3fibroblast growth factor 3 | Often (30–79%) | In 1 condition |
| FGFRL1fibroblast growth factor receptor like 1 | Often (30–79%) | In 1 condition |
| FOXL2forkhead box L2 | Often (30–79%) | In 2 conditions |
| FREM1FRAS1 related extracellular matrix 1 | Often (30–79%) | In 2 conditions |
| FUT8fucosyltransferase 8 | Often (30–79%) | In 1 condition |
| GATA4GATA binding protein 4 | Often (30–79%) | In 1 condition |
| GLI3GLI family zinc finger 3 | Often (30–79%) | In 2 conditions |
| GLULglutamate-ammonia ligase | Often (30–79%) | In 1 condition |
| GON4Lgon-4 like | Often (30–79%) | In 1 condition |
| GPC4glypican 4 | Often (30–79%) | In 1 condition |
| GPRASP2G protein-coupled receptor associated sorting protein 2 | Often (30–79%) | In 1 condition |
| HBA1hemoglobin subunit alpha 1 | Often (30–79%) | In 1 condition |
| HBA2hemoglobin subunit alpha 2 | Often (30–79%) | In 1 condition |
| HCCSholocytochrome c synthase | Often (30–79%) | In 1 condition |
| HIVEP2HIVEP zinc finger 2 | Often (30–79%) | In 1 condition |
| HNRNPKheterogeneous nuclear ribonucleoprotein K | Often (30–79%) | In 2 conditions |
| IGF1Rinsulin like growth factor 1 receptor | Often (30–79%) | In 2 conditions |
| KAT6Blysine acetyltransferase 6B | Often (30–79%) | In 1 condition |
| KATNB1katanin regulatory subunit B1 | Often (30–79%) | In 1 condition |
| KCNH1potassium voltage-gated channel subfamily H member 1 | Often (30–79%) | In 2 conditions |
| KCNJ8potassium inwardly rectifying channel subfamily J member 8 | Often (30–79%) | In 1 condition |
| KCNN3potassium calcium-activated channel subfamily N member 3 | Often (30–79%) | In 1 condition |
| KICS2KICSTOR subunit 2 | Often (30–79%) | In 1 condition |
| KIF14kinesin family member 14 | Often (30–79%) | In 1 condition |
| KNSTRNkinetochore localized astrin (SPAG5) binding protein | Often (30–79%) | In 2 conditions |
| LTBP3latent transforming growth factor beta binding protein 3 | Often (30–79%) | In 1 condition |
| MAN1B1mannosidase alpha class 1B member 1 | Often (30–79%) | In 2 conditions |
| MARS2methionyl-tRNA synthetase 2, mitochondrial | Often (30–79%) | In 1 condition |
| MED13Lmediator complex subunit 13L | Often (30–79%) | In 1 condition |
| MEGF8multiple EGF like domains 8 | Often (30–79%) | In 1 condition |
| MITFmelanocyte inducing transcription factor | Often (30–79%) | In 2 conditions |
| MKS1MKS transition zone complex subunit 1 | Often (30–79%) | In 1 condition |
| MYRFmyelin regulatory factor | Often (30–79%) | In 1 condition |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Often (30–79%) | In 1 condition |
| NECTIN1nectin cell adhesion molecule 1 | Often (30–79%) | In 1 condition |
| NEK1NIMA related kinase 1 | Often (30–79%) | In 1 condition |
| NOGnoggin | Often (30–79%) | In 1 condition |
| PACS2phosphofurin acidic cluster sorting protein 2 | Often (30–79%) | In 1 condition |
| PAN2poly(A) specific ribonuclease subunit PAN2 | Often (30–79%) | In 1 condition |
| PAX1paired box 1 | Often (30–79%) | In 1 condition |
| PCNTpericentrin | Often (30–79%) | In 1 condition |
| PIGTphosphatidylinositol glycan anchor biosynthesis class T | Often (30–79%) | In 1 condition |
| PIGYphosphatidylinositol glycan anchor biosynthesis class Y | Often (30–79%) | In 1 condition |
| PIK3C2Aphosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | Often (30–79%) | In 2 conditions |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Often (30–79%) | In 2 conditions |
| PKDCCprotein kinase domain containing, cytoplasmic | Often (30–79%) | In 1 condition |
| PLK4polo like kinase 4 | Often (30–79%) | In 1 condition |
| POLR1BRNA polymerase I subunit B | Often (30–79%) | In 1 condition |
| POLR1CRNA polymerase I and III subunit C | Often (30–79%) | In 1 condition |
| POLR1DRNA polymerase I and III subunit D | Often (30–79%) | In 1 condition |
| PPP1R21protein phosphatase 1 regulatory subunit 21 | Often (30–79%) | In 1 condition |
| PRKG2protein kinase cGMP-dependent 2 | Often (30–79%) | In 1 condition |
| PTCH1patched 1 | Often (30–79%) | In 3 conditions |
| PTCH2patched 2 | Often (30–79%) | In 1 condition |
| PTPN11protein tyrosine phosphatase non-receptor type 11 | Often (30–79%) | In 1 condition |
| PUF60poly(U) binding splicing factor 60 | Often (30–79%) | In 3 conditions |
| PUM1pumilio RNA binding family member 1 | Often (30–79%) | In 1 condition |
| QARS1glutaminyl-tRNA synthetase 1 | Often (30–79%) | In 1 condition |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Often (30–79%) | In 1 condition |
| RBM10RNA binding motif protein 10 | Often (30–79%) | In 2 conditions |
| RELNreelin | Often (30–79%) | In 1 condition |
| RHOAras homolog family member A | Often (30–79%) | In 1 condition |
| RLIMring finger protein, LIM domain interacting | Often (30–79%) | In 1 condition |
| RUNX2RUNX family transcription factor 2 | Often (30–79%) | In 1 condition |
| SETD2SET domain containing 2, histone lysine methyltransferase | Often (30–79%) | In 1 condition |
| SKIC3SKI3 subunit of superkiller complex | Often (30–79%) | In 1 condition |
| SLC12A6solute carrier family 12 member 6 | Often (30–79%) | In 1 condition |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Often (30–79%) | In 1 condition |
| SMG9SMG9 nonsense mediated mRNA decay factor | Often (30–79%) | In 2 conditions |
| SOX10SRY-box transcription factor 10 | Often (30–79%) | In 2 conditions |
| SPECC1Lsperm antigen with calponin homology and coiled-coil domains 1 like | Often (30–79%) | In 2 conditions |
| STAT3signal transducer and activator of transcription 3 | Often (30–79%) | In 1 condition |
| STRA6signaling receptor and transporter of retinol STRA6 | Often (30–79%) | In 1 condition |
| STT3ASTT3 oligosaccharyltransferase complex catalytic subunit A | Often (30–79%) | In 1 condition |
| SUFUSUFU negative regulator of hedgehog signaling | Often (30–79%) | In 1 condition |
| SUPT16HSPT16 homolog, facilitates chromatin remodeling subunit | Often (30–79%) | In 2 conditions |
| TBX6T-box transcription factor 6 | Often (30–79%) | In 1 condition |
| TCOF1treacle ribosome biogenesis factor 1 | Often (30–79%) | In 1 condition |
| TFAP2Atranscription factor AP-2 alpha | Often (30–79%) | In 1 condition |
| TNNI2troponin I2, fast skeletal type | Often (30–79%) | In 2 conditions |
| TNNT3troponin T3, fast skeletal type | Often (30–79%) | In 1 condition |
| TOE1target of EGR1, exonuclease | Often (30–79%) | In 2 conditions |
| TOGARAM1TOG array regulator of axonemal microtubules 1 | Often (30–79%) | In 1 condition |
| TPM2tropomyosin 2 | Often (30–79%) | In 1 condition |
| TPRtranslocated promoter region, nuclear basket protein | Often (30–79%) | In 1 condition |
| TRIM33tripartite motif containing 33 | Often (30–79%) | In 1 condition |
| TRIM37tripartite motif containing 37 | Often (30–79%) | In 2 conditions |
| TRMT1tRNA methyltransferase 1 | Often (30–79%) | In 1 condition |
| TUBGCP4tubulin gamma complex component 4 | Often (30–79%) | In 1 condition |
| TUBGCP6tubulin gamma complex component 6 | Often (30–79%) | In 1 condition |
| TWIST1twist family bHLH transcription factor 1 | Often (30–79%) | In 1 condition |
| UMPSuridine monophosphate synthetase | Often (30–79%) | In 1 condition |
| VPS33AVPS33A core subunit of CORVET and HOPS complexes | Often (30–79%) | In 1 condition |
| WLSWnt ligand secretion mediator | Often (30–79%) | In 1 condition |
| YARS1tyrosyl-tRNA synthetase 1 | Often (30–79%) | In 1 condition |
| ZEB2zinc finger E-box binding homeobox 2 | Often (30–79%) | In 3 conditions |
| AGO2argonaute RISC catalytic component 2 | Sometimes (5–29%) | In 1 condition |
| AHDC1AT-hook DNA binding motif containing 1 | Sometimes (5–29%) | In 1 condition |
| AP4B1adaptor related protein complex 4 subunit beta 1 | Sometimes (5–29%) | In 1 condition |
| ARMC9armadillo repeat containing 9 | Sometimes (5–29%) | In 1 condition |
| BCAS3BCAS3 microtubule associated cell migration factor | Sometimes (5–29%) | In 1 condition |
| BMP2bone morphogenetic protein 2 | Sometimes (5–29%) | In 1 condition |
| BPNT23'(2'), 5'-bisphosphate nucleotidase 2 | Sometimes (5–29%) | In 1 condition |
| BRF1BRF1 general transcription factor IIIB subunit | Sometimes (5–29%) | In 1 condition |
| CDC42cell division cycle 42 | Sometimes (5–29%) | In 2 conditions |
| CDK13cyclin dependent kinase 13 | Sometimes (5–29%) | In 1 condition |
| CHN1chimerin 1 | Sometimes (5–29%) | In 1 condition |
| COG5component of oligomeric golgi complex 5 | Sometimes (5–29%) | In 1 condition |
| CSNK2A1casein kinase 2 alpha 1 | Sometimes (5–29%) | In 1 condition |
| CTCFCCCTC-binding factor | Sometimes (5–29%) | In 1 condition |
| CTSDcathepsin D | Sometimes (5–29%) | In 1 condition |
| DCHS1dachsous cadherin-related 1 | Sometimes (5–29%) | In 2 conditions |
| DHRS3dehydrogenase/reductase 3 | Sometimes (5–29%) | In 1 condition |
| DLK1delta like non-canonical Notch ligand 1 | Sometimes (5–29%) | In 1 condition |
| EDEM3ER degradation enhancing alpha-mannosidase like protein 3 | Sometimes (5–29%) | In 1 condition |
| EXT1exostosin glycosyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| FANCLFA complementation group L | Sometimes (5–29%) | In 1 condition |
| FBXL3F-box and leucine rich repeat protein 3 | Sometimes (5–29%) | In 1 condition |
| FBXL4F-box and leucine rich repeat protein 4 | Sometimes (5–29%) | In 1 condition |
| FBXO11F-box protein 11 | Sometimes (5–29%) | In 1 condition |
| FEM1Bfem-1 homolog B | Sometimes (5–29%) | In 1 condition |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Sometimes (5–29%) | In 1 condition |
| FOXC1forkhead box C1 | Sometimes (5–29%) | In 1 condition |
| FRAS1Fraser extracellular matrix complex subunit 1 | Sometimes (5–29%) | In 2 conditions |
| FREM2FRAS1 related extracellular matrix 2 | Sometimes (5–29%) | In 1 condition |
| FRMPD4FERM and PDZ domain containing 4 | Sometimes (5–29%) | In 1 condition |
| GABBR1gamma-aminobutyric acid type B receptor subunit 1 | Sometimes (5–29%) | In 1 condition |
| GAD1glutamate decarboxylase 1 | Sometimes (5–29%) | In 1 condition |
| GNPNAT1glucosamine-phosphate N-acetyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| GRIP1glutamate receptor interacting protein 1 | Sometimes (5–29%) | In 1 condition |
| GTF3C3general transcription factor IIIC subunit 3 | Sometimes (5–29%) | In 1 condition |
| H4C5H4 clustered histone 5 | Sometimes (5–29%) | In 1 condition |
| HECTD4HECT domain E3 ubiquitin protein ligase 4 | Sometimes (5–29%) | In 1 condition |
| HNRNPRheterogeneous nuclear ribonucleoprotein R | Sometimes (5–29%) | In 1 condition |
| HS2ST1heparan sulfate 2-O-sulfotransferase 1 | Sometimes (5–29%) | In 1 condition |
| JARID2jumonji and AT-rich interaction domain containing 2 | Sometimes (5–29%) | In 1 condition |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Sometimes (5–29%) | In 1 condition |
| KCNJ5potassium inwardly rectifying channel subfamily J member 5 | Sometimes (5–29%) | In 1 condition |
| KDM2Blysine demethylase 2B | Sometimes (5–29%) | In 1 condition |
| KDM4Blysine demethylase 4B | Sometimes (5–29%) | In 1 condition |
| KIF11kinesin family member 11 | Sometimes (5–29%) | In 1 condition |
| KIFBPkinesin family binding protein | Sometimes (5–29%) | In 2 conditions |
| KITKIT proto-oncogene, receptor tyrosine kinase | Sometimes (5–29%) | In 1 condition |
| KMT5Blysine methyltransferase 5B | Sometimes (5–29%) | In 1 condition |
| KPTNkaptin, actin binding protein | Sometimes (5–29%) | In 1 condition |
| KRASKRas proto-oncogene, GTPase | Sometimes (5–29%) | In 1 condition |
| KREMEN1kringle containing transmembrane protein 1 | Sometimes (5–29%) | In 1 condition |
| LGI1leucine rich glioma inactivated 1 | Sometimes (5–29%) | In 1 condition |
| LMNB1lamin B1 | Sometimes (5–29%) | In 1 condition |
| LRPPRCleucine rich pentatricopeptide repeat containing | Sometimes (5–29%) | In 1 condition |
| LZTR1leucine zipper like post translational regulator 1 | Sometimes (5–29%) | In 1 condition |
| MAFBMAF bZIP transcription factor B | Sometimes (5–29%) | In 2 conditions |
| MAPK1mitogen-activated protein kinase 1 | Sometimes (5–29%) | In 1 condition |
| MARK2microtubule affinity regulating kinase 2 | Sometimes (5–29%) | In 1 condition |
| MECP2methyl-CpG binding protein 2 | Sometimes (5–29%) | In 1 condition |
| MEG3maternally expressed 3 | Sometimes (5–29%) | In 1 condition |
| MPV17mitochondrial inner membrane protein MPV17 | Sometimes (5–29%) | In 1 condition |
| NOTCH2notch receptor 2 | Sometimes (5–29%) | In 1 condition |
| NSUN2NOP2/Sun RNA methyltransferase 2 | Sometimes (5–29%) | In 1 condition |
| OPHN1oligophrenin 1 | Sometimes (5–29%) | In 1 condition |
| PAHphenylalanine hydroxylase | Sometimes (5–29%) | In 1 condition |
| PIGBphosphatidylinositol glycan anchor biosynthesis class B | Sometimes (5–29%) | In 2 conditions |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sometimes (5–29%) | In 2 conditions |
| PITX2paired like homeodomain 2 | Sometimes (5–29%) | In 2 conditions |
| POLR1ARNA polymerase I subunit A | Sometimes (5–29%) | In 1 condition |
| PRKDCprotein kinase, DNA-activated, catalytic subunit | Sometimes (5–29%) | In 1 condition |
| PRMT7protein arginine methyltransferase 7 | Sometimes (5–29%) | In 1 condition |
| PURApurine rich element binding protein A | Sometimes (5–29%) | In 2 conditions |
| RAB34RAB34, member RAS oncogene family | Sometimes (5–29%) | In 1 condition |
| RFX7regulatory factor X7 | Sometimes (5–29%) | In 1 condition |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Sometimes (5–29%) | In 1 condition |
| RPL10ribosomal protein L10 | Sometimes (5–29%) | In 1 condition |
| RTL1retrotransposon Gag like 1 | Sometimes (5–29%) | In 1 condition |
| RTTNrotatin | Sometimes (5–29%) | In 1 condition |
| RYR1ryanodine receptor 1 | Sometimes (5–29%) | In 1 condition |
| SALL4spalt like transcription factor 4 | Sometimes (5–29%) | In 1 condition |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Sometimes (5–29%) | In 2 conditions |
| SEPHS1selenophosphate synthetase 1 | Sometimes (5–29%) | In 1 condition |
| SETSET nuclear proto-oncogene | Sometimes (5–29%) | In 1 condition |
| SHANK3SH3 and multiple ankyrin repeat domains 3 | Sometimes (5–29%) | In 1 condition |
| SLC1A4solute carrier family 1 member 4 | Sometimes (5–29%) | In 1 condition |
| SLC35C1solute carrier family 35 member C1 | Sometimes (5–29%) | In 1 condition |
| SLC4A10solute carrier family 4 member 10 | Sometimes (5–29%) | In 1 condition |
| SNAI2snail family transcriptional repressor 2 | Sometimes (5–29%) | In 1 condition |
| SNX14sorting nexin 14 | Sometimes (5–29%) | In 1 condition |
| SONSON DNA and RNA binding protein | Sometimes (5–29%) | In 2 conditions |
| SOX6SRY-box transcription factor 6 | Sometimes (5–29%) | In 1 condition |
| SPTBN1spectrin beta, non-erythrocytic 1 | Sometimes (5–29%) | In 1 condition |
| SVBPsmall vasohibin binding protein | Sometimes (5–29%) | In 1 condition |
| TBCKTBC1 domain containing kinase | Sometimes (5–29%) | In 2 conditions |
| TMEM53transmembrane protein 53 | Sometimes (5–29%) | In 1 condition |
| TP63tumor protein p63 | Sometimes (5–29%) | In 2 conditions |
| TRIOtrio Rho guanine nucleotide exchange factor | Sometimes (5–29%) | In 1 condition |
| TRPS1transcriptional repressor GATA binding 1 | Sometimes (5–29%) | In 1 condition |
| TRPV6transient receptor potential cation channel subfamily V member 6 | Sometimes (5–29%) | In 1 condition |
| TXNL4Athioredoxin like 4A | Sometimes (5–29%) | In 1 condition |
| USP9Xubiquitin specific peptidase 9 X-linked | Sometimes (5–29%) | In 2 conditions |
| WACWW domain containing adaptor with coiled-coil | Sometimes (5–29%) | In 1 condition |
| WARS2tryptophanyl tRNA synthetase 2, mitochondrial | Sometimes (5–29%) | In 1 condition |
| ZMYM2zinc finger MYM-type containing 2 | Sometimes (5–29%) | In 1 condition |
| ZSCAN10zinc finger and SCAN domain containing 10 | Sometimes (5–29%) | In 1 condition |
| ADA2adenosine deaminase 2 | Rarely (1–4%) | In 1 condition |
| AP2M1adaptor related protein complex 2 subunit mu 1 | Rarely (1–4%) | In 1 condition |
| CHD2chromodomain helicase DNA binding protein 2 | Rarely (1–4%) | In 1 condition |
| GATA1GATA binding protein 1 | Rarely (1–4%) | In 1 condition |
| HEATR3HEAT repeat containing 3 | Rarely (1–4%) | In 1 condition |
| MED16mediator complex subunit 16 | Rarely (1–4%) | In 1 condition |
| NEXMIFneurite extension and migration factor | Rarely (1–4%) | In 1 condition |
| RNU4-2RNA, U4 small nuclear 2 | Rarely (1–4%) | In 1 condition |
| RPL11ribosomal protein L11 | Rarely (1–4%) | In 1 condition |
| RPL15ribosomal protein L15 | Rarely (1–4%) | In 1 condition |
| RPL18ribosomal protein L18 | Rarely (1–4%) | In 1 condition |
| RPL26ribosomal protein L26 | Rarely (1–4%) | In 1 condition |
| RPL27ribosomal protein L27 | Rarely (1–4%) | In 1 condition |
| RPL31ribosomal protein L31 | Rarely (1–4%) | In 1 condition |
| RPL35ribosomal protein L35 | Rarely (1–4%) | In 1 condition |
| RPL35Aribosomal protein L35a | Rarely (1–4%) | In 1 condition |
| RPL5ribosomal protein L5 | Rarely (1–4%) | In 1 condition |
| RPL8ribosomal protein L8 | Rarely (1–4%) | In 1 condition |
| RPL9ribosomal protein L9 | Rarely (1–4%) | In 1 condition |
| RPS10ribosomal protein S10 | Rarely (1–4%) | In 1 condition |
| RPS15Aribosomal protein S15a | Rarely (1–4%) | In 1 condition |
| RPS17ribosomal protein S17 | Rarely (1–4%) | In 1 condition |
| RPS19ribosomal protein S19 | Rarely (1–4%) | In 1 condition |
| RPS20ribosomal protein S20 | Rarely (1–4%) | In 1 condition |
| RPS24ribosomal protein S24 | Rarely (1–4%) | In 1 condition |
| RPS26ribosomal protein S26 | Rarely (1–4%) | In 1 condition |
| RPS27ribosomal protein S27 | Rarely (1–4%) | In 1 condition |
| RPS28ribosomal protein S28 | Rarely (1–4%) | In 1 condition |
| RPS29ribosomal protein S29 | Rarely (1–4%) | In 1 condition |
| RPS7ribosomal protein S7 | Rarely (1–4%) | In 2 conditions |
| SCN1Asodium voltage-gated channel alpha subunit 1 | Rarely (1–4%) | In 1 condition |
| SLC2A1solute carrier family 2 member 1 | Rarely (1–4%) | In 1 condition |
| SLC6A1solute carrier family 6 member 1 | Rarely (1–4%) | In 1 condition |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Rarely (1–4%) | In 1 condition |
| TSR2TSR2 ribosome maturation factor | Rarely (1–4%) | In 1 condition |
| ACOX1acyl-CoA oxidase 1 | Not recorded | In 1 condition |
| ACY1aminoacylase 1 | Not recorded | In 1 condition |
| AHI1Abelson helper integration site 1 | Not recorded | In 1 condition |
| ALG3ALG3 alpha-1,3- mannosyltransferase | Not recorded | In 1 condition |
| AP4E1adaptor related protein complex 4 subunit epsilon 1 | Not recorded | In 1 condition |
| AP4S1adaptor related protein complex 4 subunit sigma 1 | Not recorded | In 1 condition |
| ARXaristaless related homeobox | Not recorded | In 1 condition |
| ATAD3AATPase family AAA domain containing 3A | Not recorded | In 1 condition |
| ATP6V0A2ATPase H+ transporting V0 subunit a2 | Not recorded | In 1 condition |
| ATRXATRX chromatin remodeler | Not recorded | In 1 condition |
| CCNKcyclin K | Not recorded | In 1 condition |
| CD96CD96 molecule | Not recorded | In 1 condition |
| CENPFcentromere protein F | Not recorded | In 1 condition |
| CHD3chromodomain helicase DNA binding protein 3 | Not recorded | In 1 condition |
| COL27A1collagen type XXVII alpha 1 chain | Not recorded | In 1 condition |
| COLEC11collectin subfamily member 11 | Not recorded | In 1 condition |
| DDX3XDEAD-box helicase 3 X-linked | Not recorded | In 1 condition |
| EDNRAendothelin receptor type A | Not recorded | In 1 condition |
| EEDembryonic ectoderm development | Not recorded | In 1 condition |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Not recorded | In 1 condition |
| FLNBfilamin B | Not recorded | In 1 condition |
| G6PC3glucose-6-phosphatase catalytic subunit 3 | Not recorded | In 1 condition |
| GATAD2BGATA zinc finger domain containing 2B | Not recorded | In 1 condition |
| GNPATglyceronephosphate O-acyltransferase | Not recorded | In 1 condition |
| GPC6glypican 6 | Not recorded | In 1 condition |
| IFT57intraflagellar transport 57 | Not recorded | In 1 condition |
| LARP7La ribonucleoprotein 7, transcriptional regulator | Not recorded | In 1 condition |
| MAFMAF bZIP transcription factor | Not recorded | In 1 condition |
| MED13mediator complex subunit 13 | Not recorded | In 1 condition |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Not recorded | In 1 condition |
| NRASNRAS proto-oncogene, GTPase | Not recorded | In 1 condition |
| OTUD6BOTU deubiquitinase 6B | Not recorded | In 1 condition |
| PARS2prolyl-tRNA synthetase 2, mitochondrial | Not recorded | In 1 condition |
| PBX1PBX homeobox 1 | Not recorded | In 1 condition |
| PDHA1pyruvate dehydrogenase E1 subunit alpha 1 | Not recorded | In 1 condition |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Not recorded | In 1 condition |
| PUS7pseudouridine synthase 7 | Not recorded | In 1 condition |
| RALARAS like proto-oncogene A | Not recorded | In 1 condition |
| RARBretinoic acid receptor beta | Not recorded | In 1 condition |
| SOX18SRY-box transcription factor 18 | Not recorded | In 1 condition |
| SOX5SRY-box transcription factor 5 | Not recorded | In 1 condition |
| SRCAPSnf2 related CREBBP activator protein | Not recorded | In 1 condition |
| STAG2STAG2 cohesin complex component | Not recorded | In 1 condition |
| TAPT1transmembrane anterior posterior transformation 1 | Not recorded | In 1 condition |
| TCF4transcription factor 4 | Not recorded | In 1 condition |
| TENT5Aterminal nucleotidyltransferase 5A | Not recorded | In 1 condition |
| TMEM70transmembrane protein 70 | Not recorded | In 1 condition |
| TMEM94transmembrane protein 94 | Not recorded | In 1 condition |
| TNPO2transportin 2 | Not recorded | In 1 condition |
| TRRAPtransformation/transcription domain associated protein | Not recorded | In 1 condition |
| WDR35WD repeat domain 35 | Not recorded | In 1 condition |
| WNT7AWnt family member 7A | Not recorded | In 1 condition |
| ZMIZ1zinc finger MIZ-type containing 1 | Not recorded | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.19-9814e911.
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