AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Trait
Facial asymmetry
An abnormal difference between the left and right sides of the face.
Summary
- Also called
- Asymmetry of face, Crooked face, Unbalanced face, Unequal sides of face, Uneven face, Uneven sides of face, Unsymmetrical face, Asymmetric facies, Asymmetry of right and left side of face
- Body system
- Abnormality of head or neck
AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/facial-asymmetry.json"
page <- fromJSON(url)
page$trait$nameFacial asymmetryHP:0000324
AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
Read the genes linked to Facial asymmetry, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test107 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 →
- DNA Repair DiseaseReads 18 of these genesBRCA1BRCA2BRIP1ERCC4FANCAFANCBAbout this report →
- Multiple Synostoses Syndrome (FGF9)Reads 4 of these genesGDF6FGF9GDF5NOGAbout this report →
- Branchio-Oto-Renal Spectrum DisorderReads 3 of these genesEYA1SIX1SIX5About this report →
Show 103 more reports
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Syndromic CraniosynostosisReads 5 of these genesFGFR2FGFR3TWIST1KAT6ASMOAbout this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 3 of these genesBRIP1PALB2RAD51CAbout this report →
- Achondrogenesis panelReads 2 of these genesCOL2A1GDF5About this report →
- Auriculocondylar Syndrome 2 (PLCB4)Reads 1 of these genesPLCB4About this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- Blepharocheilodontic Syndrome 2 (CTNND1)Reads 1 of these genesCTNND1About this report →
- BMP4-Related Microphthalmia and AnophthalmiaReads 1 of these genesBMP4About this report →
- Caffey DiseaseReads 1 of these genesCOL1A1About this report →
- Cenani-Lenz Syndactyly SyndromeReads 1 of these genesLRP4About this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- CHRNG-Related Multiple Pterygium SyndromeReads 1 of these genesCHRNGAbout this report →
- Craniofrontonasal SyndromeReads 1 of these genesEFNB1About this report →
- Curry-Jones Syndrome (Mosaic SMO Syndrome)Reads 1 of these genesSMOAbout this report →
- EBF3-Related Neurodevelopmental Disorder (HADDS)Reads 1 of these genesEBF3About this report →
- Elsahy-Waters SyndromeReads 1 of these genesCDH11About this report →
- FANCM-Related Genomic Instability DisorderReads 1 of these genesFANCMAbout this report →
- Feingold Syndrome Type 1Reads 1 of these genesMYCNAbout this report →
- Ferguson-Smith Disease (Multiple Self-Healing Squamous Epithelioma)Reads 1 of these genesTGFBR1About this report →
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- Focal Dermal Hypoplasia (Goltz Syndrome)Reads 1 of these genesPORCNAbout this report →
- Lamb-Shaffer SyndromeReads 1 of these genesSOX5About this report →
- Marshall-Smith SyndromeReads 1 of these genesNFIXAbout this report →
- MEND SyndromeReads 1 of these genesEBPAbout this report →
- Mucopolysaccharidosis Type VII (Sly Syndrome)Reads 1 of these genesGUSBAbout this report →
- NOG-Related Symphalangism Spectrum DisorderReads 1 of these genesNOGAbout this report →
- OFD1-Related CiliopathyReads 1 of these genesOFD1About this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- SF3B4-Related Acrofacial Dysostosis (Nager Syndrome)Reads 1 of these genesSF3B4About this report →
- Stankiewicz-Isidor SyndromeReads 1 of these genesPSMD12About this report →
- Townes-Brocks SyndromeReads 1 of these genesSALL1About this report →
- Wiedemann-Steiner SyndromeReads 1 of these genesKMT2AAbout this report →
- ZIC1-Related CraniosynostosisReads 1 of these genesZIC1About this report →
- ZTTK SyndromeReads 1 of these genesSONAbout this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 3 of these genesEYA1SIX1SIX5About this report →
- Hypertrophic CardiomyopathyReads 7 of these genesH19HRASIGF2KRASNRASDHX37About this report →
- Noonan SyndromeReads 4 of these genesHRASKRASNRASMAPK1About this report →
- Cornelia de Lange SyndromeReads 2 of these genesSMC1ASMC3About this report →
- Congenital Cranial Dysinnervation DisordersReads 2 of these genesCHN1MAFBAbout this report →
- Intellectual DisabilityReads 11 of these genesSMSKAT6ASATB2TRIOCDK13KDM4BAbout this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesAKT1About this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Kabuki SyndromeReads 1 of these genesKMT2DAbout this report →
- Otospondylomegaepiphyseal Dysplasia (OSMED)Reads 1 of these genesCOL2A1About this report →
- Severe Inherited Insulin ResistanceReads 1 of these genesAKT2About this report →
- STAT1 and STAT3 Gain-of-Function DiseaseReads 1 of these genesSTAT3About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 2 of these genesCOL2A1FN1About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 2 of these genesH19IGF2About this report →
- Autoimmune DiseaseReads 3 of these genesCHRNGKRASSTAT3About this report →
- Familial Periodic ParalysisReads 1 of these genesKCNJ2About this report →
- Fraser SyndromeReads 1 of these genesFRAS1About this report →
- Stargardt DiseaseReads 1 of these genesELOVL4About this report →
- Osteogenesis ImperfectaReads 3 of these genesSP7NBASCOL1A1About this report →
- Familial Atrial FibrillationReads 1 of these genesKCNJ2About this report →
- NeurofibromatosisReads 1 of these genesNF1About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNFIXAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesGNASAbout this report →
- Short Qt SyndromeReads 1 of these genesKCNJ2About this report →
- Treacher Collins SyndromeReads 1 of these genesPOLR1BAbout this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Ehlers-Danlos SyndromeReads 2 of these genesCHST14COL1A1About this report →
- Lissencephaly Spectrum DisordersReads 2 of these genesCEP85LMACF1About this report →
- Syndromic Complex Neurodevelopmental DisorderReads 2 of these genesTRPM3RNU4-2About this report →
- Hereditary Orofacial CleftingReads 1 of these genesBMP4About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Heritable Pulmonary Arterial Hypertension (HPAH)Reads 1 of these genesKCNK3About this report →
- Loeys-Dietz SyndromeReads 1 of these genesTGFBR1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 2 of these genesSMOGLI2About this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Hyper-IgE SyndromeReads 1 of these genesSTAT3About this report →
- Epilepsy (Full Panel)Reads 5 of these genesPIGARNU2-2FLNASMC1ANTRK2About this report →
- Long QT SyndromeReads 1 of these genesKCNJ2About this report →
- Marfan Like SyndromesReads 1 of these genesTGFBR1About this report →
- Congenital Disorders of GlycosylationReads 3 of these genesCHST14PIGASLC37A4About this report →
- Polycystic Kidney DiseaseReads 1 of these genesPKD2About this report →
- LipodystrophyReads 1 of these genesAKT2About this report →
- Hypogonadotropic HypogonadismReads 2 of these genesCHD7ANOS1About this report →
- Aortic AneurysmReads 1 of these genesTGFBR1About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesFLNAAbout this report →
- Glycogen Storage DiseaseReads 1 of these genesSLC37A4About this report →
- Monogenic Hypertension & Mineralocorticoid DisordersReads 1 of these genesKCNJ5About this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesCEP152About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesDHX37About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGAAbout this report →
- Other Inborn Errors of ImmunityReads 3 of these genesKRASNBASSTAT3About this report →
- Congenital Myasthenic SyndromeReads 1 of these genesLRP4About this report →
- VitreoretinopathyReads 1 of these genesCOL2A1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBMP4About this report →
- Diabetes MellitusReads 1 of these genesAKT2About this report →
- Thyroid CancerReads 1 of these genesGNASAbout this report →
- Inherited ThrombocytopeniasReads 1 of these genesFLI1About this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesELOVL4About this report →
- Joubert Syndrome And Related DisordersReads 1 of these genesOFD1About this report →
- Male InfertilityReads 1 of these genesFANCMAbout this report →
- Female InfertilityReads 1 of these genesFANCMAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 2 of these genesSEPTIN9SLC12A6About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGUSBAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesSLC12A6About this report →
- Retinitis PigmentosaReads 1 of these genesOFD1About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesELOVL4SLC12A6About this report →
- Hearing Loss and DeafnessReads 1 of these genesSIX1About this report →
Read the genes linked to Facial asymmetry, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test153 genes linked to Facial asymmetry
Changes in these genes cause rare conditions in which Facial asymmetry 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 |
|---|---|---|
| CHST14carbohydrate sulfotransferase 14 | Always | In 1 condition |
| DHRS3dehydrogenase/reductase 3 | Always | In 1 condition |
| ELMO2engulfment and cell motility 2 | Always | In 1 condition |
| GUSBglucuronidase beta | Always | In 1 condition |
| KCNK3potassium two pore domain channel subfamily K member 3 | Always | In 1 condition |
| NEUROG1neurogenin 1 | Always | In 1 condition |
| PIGAphosphatidylinositol glycan anchor biosynthesis class A | Always | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Always | In 5 conditions |
| RHOAras homolog family member A | Always | In 1 condition |
| RNU2-2RNA, U2 small nuclear 2 | Always | In 1 condition |
| SF3B4splicing factor 3b subunit 4 | Always | In 1 condition |
| SLC37A4solute carrier family 37 member 4 | Always | In 1 condition |
| SMSspermine synthase | Always | In 2 conditions |
| SP7Sp7 transcription factor | Always | In 1 condition |
| TGFBR1transforming growth factor beta receptor 1 | Always | In 1 condition |
| TM2D3TM2 domain containing 3 | Always | In 1 condition |
| FGFR2fibroblast growth factor receptor 2 | Very often (80–99%) | In 3 conditions |
| FGFR3fibroblast growth factor receptor 3 | Very often (80–99%) | In 1 condition |
| GDF3growth differentiation factor 3 | Very often (80–99%) | In 1 condition |
| GDF6growth differentiation factor 6 | Very often (80–99%) | In 3 conditions |
| MEOX1mesenchyme homeobox 1 | Very often (80–99%) | In 1 condition |
| PORCNporcupine O-acyltransferase | Very often (80–99%) | In 2 conditions |
| TWIST1twist family bHLH transcription factor 1 | Very often (80–99%) | In 2 conditions |
| AKT2AKT serine/threonine kinase 2 | Often (30–79%) | In 1 condition |
| ASPHaspartate beta-hydroxylase | Often (30–79%) | In 1 condition |
| CHD7chromodomain helicase DNA binding protein 7 | Often (30–79%) | In 2 conditions |
| CHRNGcholinergic receptor nicotinic gamma subunit | Often (30–79%) | In 1 condition |
| DDX59DEAD-box helicase 59 | Often (30–79%) | In 1 condition |
| EBPEBP cholestenol delta-isomerase | Often (30–79%) | In 1 condition |
| EDN1endothelin 1 | Often (30–79%) | In 1 condition |
| EFNB1ephrin B1 | Often (30–79%) | In 2 conditions |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Often (30–79%) | In 1 condition |
| FLNAfilamin A | Often (30–79%) | In 1 condition |
| FRAS1Fraser extracellular matrix complex subunit 1 | Often (30–79%) | In 1 condition |
| GNAI3G protein subunit alpha i3 | Often (30–79%) | In 1 condition |
| GON4Lgon-4 like | Often (30–79%) | In 1 condition |
| H19H19 imprinted maternally expressed transcript | Often (30–79%) | In 2 conditions |
| HDAC9histone deacetylase 9 | Often (30–79%) | In 1 condition |
| HRASHRas proto-oncogene, GTPase | Often (30–79%) | In 1 condition |
| IGF2insulin like growth factor 2 | Often (30–79%) | In 2 conditions |
Show 113 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| KAT6Alysine acetyltransferase 6A | Often (30–79%) | In 1 condition |
| KCNQ1OT1KCNQ1 opposite strand/antisense transcript 1 | Often (30–79%) | In 1 condition |
| KMT2Alysine methyltransferase 2A | Often (30–79%) | In 1 condition |
| KRASKRas proto-oncogene, GTPase | Often (30–79%) | In 2 conditions |
| LRP4LDL receptor related protein 4 | Often (30–79%) | In 1 condition |
| MYH3myosin heavy chain 3 | Often (30–79%) | In 1 condition |
| NBASNBAS subunit of NRZ tethering complex | Often (30–79%) | In 1 condition |
| NRASNRAS proto-oncogene, GTPase | Often (30–79%) | In 1 condition |
| OFD1OFD1 centriole and centriolar satellite protein | Often (30–79%) | In 2 conditions |
| PLCB4phospholipase C beta 4 | Often (30–79%) | In 1 condition |
| POLR1BRNA polymerase I subunit B | Often (30–79%) | In 1 condition |
| PPP2R1Aprotein phosphatase 2 scaffold subunit Aalpha | Often (30–79%) | In 2 conditions |
| PSMD12proteasome 26S subunit, non-ATPase 12 | Often (30–79%) | In 1 condition |
| SATB2SATB homeobox 2 | Often (30–79%) | In 3 conditions |
| SCARF2scavenger receptor class F member 2 | Often (30–79%) | In 1 condition |
| SEMA3Esemaphorin 3E | Often (30–79%) | In 1 condition |
| SF3B2splicing factor 3b subunit 2 | Often (30–79%) | In 1 condition |
| SMOsmoothened, frizzled class receptor | Often (30–79%) | In 2 conditions |
| STAT3signal transducer and activator of transcription 3 | Often (30–79%) | In 1 condition |
| TRIOtrio Rho guanine nucleotide exchange factor | Often (30–79%) | In 2 conditions |
| YY1YY1 transcription factor | Often (30–79%) | In 2 conditions |
| ZSCAN10zinc finger and SCAN domain containing 10 | Often (30–79%) | In 1 condition |
| ADAT3adenosine deaminase tRNA specific 3 | Sometimes (5–29%) | In 1 condition |
| AKT1AKT serine/threonine kinase 1 | Sometimes (5–29%) | In 1 condition |
| ANOS1anosmin 1 | Sometimes (5–29%) | In 1 condition |
| BCRBCR activator of RhoGEF and GTPase | Sometimes (5–29%) | In 1 condition |
| BRCA1BRCA1 DNA repair associated | Sometimes (5–29%) | In 1 condition |
| BRCA2BRCA2 DNA repair associated | Sometimes (5–29%) | In 1 condition |
| BRIP1BRCA1 interacting DNA helicase 1 | Sometimes (5–29%) | In 1 condition |
| CDK13cyclin dependent kinase 13 | Sometimes (5–29%) | In 1 condition |
| CEP152centrosomal protein 152 | Sometimes (5–29%) | In 1 condition |
| CEP85Lcentrosomal protein 85L | Sometimes (5–29%) | In 1 condition |
| CHN1chimerin 1 | Sometimes (5–29%) | In 1 condition |
| CLTCL1clathrin heavy chain like 1 | Sometimes (5–29%) | In 1 condition |
| COL1A1collagen type I alpha 1 chain | Sometimes (5–29%) | In 1 condition |
| COL2A1collagen type II alpha 1 chain | Sometimes (5–29%) | In 1 condition |
| CRKLCRK like proto-oncogene, adaptor protein | Sometimes (5–29%) | In 1 condition |
| DACT1dishevelled binding antagonist of beta catenin 1 | Sometimes (5–29%) | In 1 condition |
| DHX37DEAH-box helicase 37 | Sometimes (5–29%) | In 1 condition |
| EBF3EBF transcription factor 3 | Sometimes (5–29%) | In 1 condition |
| ELOVL4ELOVL fatty acid elongase 4 | Sometimes (5–29%) | In 1 condition |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Sometimes (5–29%) | In 1 condition |
| EYA1EYA transcriptional coactivator and phosphatase 1 | Sometimes (5–29%) | In 2 conditions |
| FAAP100FA core complex associated protein 100 | Sometimes (5–29%) | In 1 condition |
| FANCAFA complementation group A | Sometimes (5–29%) | In 1 condition |
| FANCBFA complementation group B | Sometimes (5–29%) | In 1 condition |
| FANCCFA complementation group C | Sometimes (5–29%) | In 1 condition |
| FANCD2FA complementation group D2 | Sometimes (5–29%) | In 1 condition |
| FANCEFA complementation group E | Sometimes (5–29%) | In 1 condition |
| FANCFFA complementation group F | Sometimes (5–29%) | In 1 condition |
| FANCGFA complementation group G | Sometimes (5–29%) | In 1 condition |
| FANCIFA complementation group I | Sometimes (5–29%) | In 1 condition |
| FANCLFA complementation group L | Sometimes (5–29%) | In 1 condition |
| FANCMFA complementation group M | Sometimes (5–29%) | In 1 condition |
| FGF9fibroblast growth factor 9 | Sometimes (5–29%) | In 1 condition |
| FN1fibronectin 1 | Sometimes (5–29%) | In 1 condition |
| GDF5growth differentiation factor 5 | Sometimes (5–29%) | In 1 condition |
| GLI2GLI family zinc finger 2 | Sometimes (5–29%) | In 1 condition |
| GNASGNAS complex locus | Sometimes (5–29%) | In 2 conditions |
| GTF3C3general transcription factor IIIC subunit 3 | Sometimes (5–29%) | In 1 condition |
| IDH1isocitrate dehydrogenase (NADP(+)) 1 | Sometimes (5–29%) | In 1 condition |
| IDH2isocitrate dehydrogenase (NADP(+)) 2 | Sometimes (5–29%) | In 1 condition |
| KCNJ2potassium inwardly rectifying channel subfamily J member 2 | Sometimes (5–29%) | In 2 conditions |
| 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 |
| KMT2Dlysine methyltransferase 2D | Sometimes (5–29%) | In 1 condition |
| MACF1microtubule actin crosslinking factor 1 | Sometimes (5–29%) | In 1 condition |
| MAD2L2mitotic arrest deficient 2 like 2 | Sometimes (5–29%) | In 1 condition |
| MAFBMAF bZIP transcription factor B | Sometimes (5–29%) | In 1 condition |
| MAN2C1mannosidase alpha class 2C member 1 | Sometimes (5–29%) | In 1 condition |
| MAPK1mitogen-activated protein kinase 1 | Sometimes (5–29%) | In 1 condition |
| NF1neurofibromin 1 | Sometimes (5–29%) | In 1 condition |
| NFIXnuclear factor I X | Sometimes (5–29%) | In 1 condition |
| NOGnoggin | Sometimes (5–29%) | In 1 condition |
| PALB2partner and localizer of BRCA2 | Sometimes (5–29%) | In 1 condition |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Sometimes (5–29%) | In 2 conditions |
| PKD2polycystin 2, transient receptor potential cation channel | Sometimes (5–29%) | In 1 condition |
| POLR1ARNA polymerase I subunit A | Sometimes (5–29%) | In 1 condition |
| PTH1Rparathyroid hormone 1 receptor | Sometimes (5–29%) | In 2 conditions |
| PURApurine rich element binding protein A | Sometimes (5–29%) | In 1 condition |
| RAD51RAD51 recombinase | Sometimes (5–29%) | In 1 condition |
| RAD51CRAD51 paralog C | Sometimes (5–29%) | In 1 condition |
| RFWD3ring finger and WD repeat domain 3 | Sometimes (5–29%) | In 1 condition |
| RFX7regulatory factor X7 | Sometimes (5–29%) | In 1 condition |
| SALL1spalt like transcription factor 1 | Sometimes (5–29%) | In 1 condition |
| SALL4spalt like transcription factor 4 | Sometimes (5–29%) | In 2 conditions |
| SETSET nuclear proto-oncogene | Sometimes (5–29%) | In 1 condition |
| SIN3ASIN3 transcription regulator family member A | Sometimes (5–29%) | In 2 conditions |
| SIX1SIX homeobox 1 | Sometimes (5–29%) | In 2 conditions |
| SIX5SIX homeobox 5 | Sometimes (5–29%) | In 1 condition |
| SLX4SLX4 structure-specific endonuclease subunit | Sometimes (5–29%) | In 1 condition |
| SMC1Astructural maintenance of chromosomes 1A | Sometimes (5–29%) | In 1 condition |
| SMC3structural maintenance of chromosomes 3 | Sometimes (5–29%) | In 1 condition |
| SONSON DNA and RNA binding protein | Sometimes (5–29%) | In 2 conditions |
| TRPM3transient receptor potential cation channel subfamily M member 3 | Sometimes (5–29%) | In 1 condition |
| UBE2Tubiquitin conjugating enzyme E2 T | Sometimes (5–29%) | In 1 condition |
| USP9Xubiquitin specific peptidase 9 X-linked | Sometimes (5–29%) | In 2 conditions |
| XRCC2X-ray repair cross complementing 2 | Sometimes (5–29%) | In 1 condition |
| CDH11cadherin 11 | Rarely (1–4%) | In 1 condition |
| CTNND1catenin delta 1 | Rarely (1–4%) | In 1 condition |
| PPP2R5Dprotein phosphatase 2 regulatory subunit B'delta | Rarely (1–4%) | In 1 condition |
| RNU4-2RNA, U4 small nuclear 2 | Rarely (1–4%) | In 1 condition |
| ATRATR checkpoint kinase | Not recorded | In 1 condition |
| BMP4bone morphogenetic protein 4 | Not recorded | In 1 condition |
| EDNRAendothelin receptor type A | Not recorded | In 1 condition |
| MYCNMYCN proto-oncogene, bHLH transcription factor | Not recorded | In 1 condition |
| MYH8myosin heavy chain 8 | Not recorded | In 1 condition |
| NTRK2neurotrophic receptor tyrosine kinase 2 | Not recorded | In 1 condition |
| SEPTIN9septin 9 | Not recorded | In 1 condition |
| SLC12A6solute carrier family 12 member 6 | Not recorded | In 1 condition |
| SOX5SRY-box transcription factor 5 | Not recorded | In 1 condition |
| ZIC1Zic family zinc finger 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.
Narrower traits
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.
AtlasWho We HelpOur ScienceProductsOutcomes
Log InAskSequence your genome↗
From traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 810+ physician-ready reports.
From $449
Free shipping · Results in 6–8 weeks
