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Trait
Abnormally shaped ears
Clinical name: Abnormal pinna morphology
An abnormality of the pinna, which is also referred to as the auricle or external ear.
Summary
- Also called
- Auricular malformation, Deformed ears, Malformed ears, Abnormal form of ears, Deformed auricles, Dysplastic ears, Malformation of auricle, Malformed auricles, Malformed external ears, Minor malformation of the auricles, Poorly defined conchae
- Body system
- Abnormality of the ear
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Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/abnormal-pinna-morphology.json"
page <- fromJSON(url)
page$trait$nameAbnormally shaped earsHP:0000377
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Get my Genome Test90 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 →
- Zellweger Spectrum & Peroxisome Biogenesis DisordersReads 13 of these genesPEX1PEX10PEX11BPEX12PEX13PEX14About this report →
- DNA Repair DiseaseReads 20 of these genesBRCA1BRCA2BRIP1ERCC4FANCAFANCBAbout this report →
- Agammaglobulinaemia (XLA and Autosomal Forms)Reads 8 of these genesBLNKCD79ACD79BIGHMIGLL1PIK3R1About this report →
Show 86 more reports
- Branchio-Oto-Renal Spectrum DisorderReads 3 of these genesEYA1SIX1SIX5About this report →
- Fraser SyndromeReads 3 of these genesFRAS1FREM2GRIP1About this report →
- Other Inherited LeukodystrophiesReads 13 of these genesPEX1PEX10PEX11BPEX12PEX13PEX14About this report →
- Activated PI3K-Delta Syndrome (APDS)Reads 2 of these genesPIK3CDPIK3R1About this report →
- Hereditary Breast and Ovarian Cancer (BRCA1/2)Reads 2 of these genesBRCA1BRCA2About this report →
- Syndromic CraniosynostosisReads 6 of these genesFGFR2FGFR3TWIST1PORRAB23SKIAbout this report →
- Inherited Neurodegenerative DisordersReads 21 of these genesPEX1PEX10PEX11BPEX12PEX13PEX14About this report →
- Primary Lymphoedema & Lymphatic MalformationsReads 4 of these genesADAMTS3CCBE1FAT4PIEZO1About this report →
- Breast and Ovarian Cancer Genes Beyond BRCA1/2Reads 3 of these genesBRIP1PALB2RAD51CAbout this report →
- 3MC Syndrome 1 (MASP1)Reads 1 of these genesMASP1About this report →
- Aarskog-Scott SyndromeReads 1 of these genesFGD1About this report →
- Auriculocondylar Syndrome 2 (PLCB4)Reads 1 of these genesPLCB4About this report →
- Basilicata-Akhtar SyndromeReads 1 of these genesMSL3About this report →
- Bent Bone Dysplasia Syndrome (FGFR2)Reads 1 of these genesFGFR2About this report →
- CEBALID Syndrome (MN1)Reads 1 of these genesMN1About this report →
- CHARGE SyndromeReads 1 of these genesCHD7About this report →
- CystathioninuriaReads 1 of these genesCTHAbout this report →
- DeSanto-Shinawi SyndromeReads 1 of these genesWACAbout this report →
- FANCM-Related Genomic Instability DisorderReads 1 of these genesFANCMAbout this report →
- FAT4-Related Neurodevelopmental DisorderReads 1 of these genesFAT4About this report →
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- INTU-Related Skeletal CiliopathyReads 1 of these genesINTUAbout this report →
- Kaufman Oculocerebrofacial SyndromeReads 1 of these genesUBE3BAbout this report →
- MEND SyndromeReads 1 of these genesEBPAbout this report →
- Nail-Patella SyndromeReads 1 of these genesLMX1BAbout this report →
- PALB2 related diseasesReads 1 of these genesPALB2About this report →
- PBX1-Related Kidney and Urinary Tract AnomaliesReads 1 of these genesPBX1About this report →
- PIK3R1-Related DisordersReads 1 of these genesPIK3R1About this report →
- Raine SyndromeReads 1 of these genesFAM20CAbout this report →
- Roberts SyndromeReads 1 of these genesESCO2About this report →
- SF3B4-Related Acrofacial Dysostosis (Nager Syndrome)Reads 1 of these genesSF3B4About this report →
- Townes-Brocks SyndromeReads 1 of these genesSALL1About this report →
- TRAPPC9-Related Intellectual DisabilityReads 1 of these genesTRAPPC9About this report →
- Rare Hereditary Peripheral NeuropathiesReads 15 of these genesPEX1PEX10PEX11BPEX12PEX13PEX14About this report →
- Intellectual DisabilityReads 15 of these genesARID1ADDX3XARID1BMED12NAA10NSD2About this report →
- Congenital Anomalies of the Kidney and Urinary TractReads 3 of these genesEYA1SIX1SIX5About this report →
- Congenital Cranial Dysinnervation DisordersReads 2 of these genesCHN1MAFBAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 3 of these genesETFAETFBETFDHAbout this report →
- Wolfram Syndrome & WFS1 SpectrumReads 1 of these genesWFS1About this report →
- Ehlers-Danlos SyndromeReads 3 of these genesCHST14DSEPLOD1About this report →
- Other Inborn Errors of ImmunityReads 9 of these genesBLNKCD79ACD79BIGHMIGLL1PIK3CDAbout this report →
- Arrhythmogenic CardiomyopathyReads 2 of these genesDSPJUPAbout this report →
- Coffin-Siris SyndromeReads 2 of these genesARID1AARID1BAbout this report →
- Inherited Congenital Heart DefectsReads 2 of these genesFLNAGATA4About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 2 of these genesTUBG1TUBBAbout this report →
- Epilepsy (Full Panel)Reads 7 of these genesDOCK7FLNACPLX1FRMPD4STXBP1OTUD6BAbout this report →
- Congenital Disorders of GlycosylationReads 5 of these genesCHST14DSEALG3ALG12PMM2About this report →
- Achondrogenesis panelReads 1 of these genesSLC26A2About this report →
- Treacher Collins SyndromeReads 1 of these genesTCOF1About this report →
- TubulinopathiesReads 1 of these genesTUBBAbout this report →
- Epidermolysis BullosaReads 2 of these genesDSPJUPAbout this report →
- Neonatal Diabetes MellitusReads 2 of these genesGATA4PTF1AAbout this report →
- Periventricular Nodular HeterotopiaReads 1 of these genesFLNAAbout this report →
- Lissencephaly Spectrum DisordersReads 2 of these genesTUBG1ACTG1About this report →
- Hereditary SpherocytosisReads 1 of these genesANK1About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesFLNAAbout this report →
- Hearing Loss and DeafnessReads 4 of these genesSIX1WFS1ACTG1COL11A1About this report →
- Hypertrophic CardiomyopathyReads 3 of these genesETFAETFBETFDHAbout this report →
- Congenital Adrenal HyperplasiaReads 1 of these genesPORAbout this report →
- Diabetes MellitusReads 2 of these genesGATA4PTF1AAbout this report →
- Red Blood Cell Membrane DisordersReads 1 of these genesPIEZO1About this report →
- Hereditary Palmoplantar Keratodermas and Pachyonychia CongenitaReads 2 of these genesGJA1DSPAbout this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesEMC1About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 1 of these genesSLC26A2About this report →
- Joubert Syndrome And Related DisordersReads 2 of these genesKIF7B9D2About this report →
- Marfan Like SyndromesReads 1 of these genesSKIAbout this report →
- Meckel SyndromeReads 1 of these genesB9D2About this report →
- HyperinsulinismReads 1 of these genesPMM2About this report →
- Hypogonadotropic HypogonadismReads 2 of these genesCHD7SMCHD1About this report →
- Female InfertilityReads 2 of these genesFANCMTP63About this report →
- Cutis LaxaReads 1 of these genesEFEMP2About this report →
- Hereditary Spastic ParaplegiaReads 2 of these genesNIPA1ERLIN2About this report →
- Ectodermal DysplasiasReads 1 of these genesTP63About this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesGATA4About this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGBAbout this report →
- Pontocerebellar Hypoplasia (TSEN54 and MINPP1)Reads 1 of these genesAMPD2About this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesWFS1About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesCNOT1About this report →
- VitreoretinopathyReads 1 of these genesCOL11A1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 1 of these genesBCORAbout this report →
- Spinal Muscular AtrophyReads 1 of these genesBICD2About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesFIG4About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesVAC14About this report →
- Male InfertilityReads 1 of these genesFANCMAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesPEX6About this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesFIG4About this report →
Read the genes linked to Abnormally shaped ears, and the rest of your genome, with one test.
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Get my Genome Test176 genes linked to Abnormally shaped ears
Changes in these genes cause rare conditions in which Abnormally shaped ears 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 |
|---|---|---|
| ARID1AAT-rich interaction domain 1A | Always | In 1 condition |
| CACHD1cache domain containing 1 | Always | In 1 condition |
| DOCK7dedicator of cytokinesis 7 | Always | In 1 condition |
| EFEMP2EGF-like fibulin extracellular matrix protein 2 | Always | In 1 condition |
| MN1MN1 proto-oncogene, transcriptional regulator | Always | In 1 condition |
| SF3B4splicing factor 3b subunit 4 | Always | In 1 condition |
| TCOF1treacle ribosome biogenesis factor 1 | Always | In 1 condition |
| VSX1visual system homeobox 1 | Always | In 1 condition |
| ADAMTS3ADAM metallopeptidase with thrombospondin type 1 motif 3 | Very often (80–99%) | In 1 condition |
| CCBE1collagen and calcium binding EGF domains 1 | Very often (80–99%) | In 1 condition |
| CHD7chromodomain helicase DNA binding protein 7 | Very often (80–99%) | In 1 condition |
| CHST14carbohydrate sulfotransferase 14 | Very often (80–99%) | In 1 condition |
| DACT1dishevelled binding antagonist of beta catenin 1 | Very often (80–99%) | In 1 condition |
| DDX3XDEAD-box helicase 3 X-linked | Very often (80–99%) | In 1 condition |
| DSEdermatan sulfate epimerase | Very often (80–99%) | In 1 condition |
| EIF4A3eukaryotic translation initiation factor 4A3 | Very often (80–99%) | In 1 condition |
| FAT4FAT atypical cadherin 4 | Very often (80–99%) | In 1 condition |
| FLNAfilamin A | Very often (80–99%) | In 1 condition |
| IGBP1immunoglobulin binding protein 1 | Very often (80–99%) | In 1 condition |
| KIF7kinesin family member 7 | Very often (80–99%) | In 1 condition |
| PEX1peroxisomal biogenesis factor 1 | Very often (80–99%) | In 1 condition |
| PEX10peroxisomal biogenesis factor 10 | Very often (80–99%) | In 1 condition |
| PEX11Bperoxisomal biogenesis factor 11 beta | Very often (80–99%) | In 1 condition |
| PEX12peroxisomal biogenesis factor 12 | Very often (80–99%) | In 1 condition |
| PEX13peroxisomal biogenesis factor 13 | Very often (80–99%) | In 1 condition |
| PEX14peroxisomal biogenesis factor 14 | Very often (80–99%) | In 1 condition |
| PEX16peroxisomal biogenesis factor 16 | Very often (80–99%) | In 1 condition |
| PEX19peroxisomal biogenesis factor 19 | Very often (80–99%) | In 1 condition |
| PEX2peroxisomal biogenesis factor 2 | Very often (80–99%) | In 1 condition |
| PEX26peroxisomal biogenesis factor 26 | Very often (80–99%) | In 1 condition |
| PEX3peroxisomal biogenesis factor 3 | Very often (80–99%) | In 1 condition |
| PEX5peroxisomal biogenesis factor 5 | Very often (80–99%) | In 1 condition |
| PEX6peroxisomal biogenesis factor 6 | Very often (80–99%) | In 1 condition |
| SALL1spalt like transcription factor 1 | Very often (80–99%) | In 1 condition |
| SEMA3Esemaphorin 3E | Very often (80–99%) | In 1 condition |
| TBCEtubulin folding cofactor E | Very often (80–99%) | In 1 condition |
| TFAP2Atranscription factor AP-2 alpha | Very often (80–99%) | In 1 condition |
| ZNHIT3zinc finger HIT-type containing 3 | Very often (80–99%) | In 1 condition |
| ALG3ALG3 alpha-1,3- mannosyltransferase | Often (30–79%) | In 1 condition |
| ANK1ankyrin 1 | Often (30–79%) | In 1 condition |
Show 136 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| ARID1BAT-rich interaction domain 1B | Often (30–79%) | In 2 conditions |
| BCORBCL6 corepressor | Often (30–79%) | In 2 conditions |
| CHRNA7cholinergic receptor nicotinic alpha 7 subunit | Often (30–79%) | In 1 condition |
| CPLX1complexin 1 | Often (30–79%) | In 1 condition |
| CTBP1C-terminal binding protein 1 | Often (30–79%) | In 1 condition |
| DLX5distal-less homeobox 5 | Often (30–79%) | In 1 condition |
| DONSONDNA replication fork stabilization factor DONSON | Often (30–79%) | In 1 condition |
| EDN1endothelin 1 | Often (30–79%) | In 1 condition |
| ESCO2establishment of sister chromatid cohesion N-acetyltransferase 2 | Often (30–79%) | In 2 conditions |
| EYA1EYA transcriptional coactivator and phosphatase 1 | Often (30–79%) | In 1 condition |
| FGD1FYVE, RhoGEF and PH domain containing 1 | Often (30–79%) | In 1 condition |
| FGF10fibroblast growth factor 10 | Often (30–79%) | In 1 condition |
| FGFR2fibroblast growth factor receptor 2 | Often (30–79%) | In 3 conditions |
| FGFR3fibroblast growth factor receptor 3 | Often (30–79%) | In 2 conditions |
| FGFRL1fibroblast growth factor receptor like 1 | Often (30–79%) | In 1 condition |
| FIG4FIG4 phosphoinositide 5-phosphatase | Often (30–79%) | In 1 condition |
| FRAS1Fraser extracellular matrix complex subunit 1 | Often (30–79%) | In 1 condition |
| FREM2FRAS1 related extracellular matrix 2 | Often (30–79%) | In 1 condition |
| GATA4GATA binding protein 4 | Often (30–79%) | In 1 condition |
| GJA1gap junction protein alpha 1 | Often (30–79%) | In 2 conditions |
| GNAI3G protein subunit alpha i3 | Often (30–79%) | In 1 condition |
| GRIP1glutamate receptor interacting protein 1 | Often (30–79%) | In 1 condition |
| HOXA2homeobox A2 | Often (30–79%) | In 1 condition |
| HYLS1HYLS1 centriolar and ciliogenesis associated | Often (30–79%) | In 1 condition |
| KLF13KLF transcription factor 13 | Often (30–79%) | In 1 condition |
| LETM1leucine zipper and EF-hand containing transmembrane protein 1 | Often (30–79%) | In 1 condition |
| MED12mediator complex subunit 12 | Often (30–79%) | In 1 condition |
| MSL3MSL complex subunit 3 | Often (30–79%) | In 1 condition |
| NAA10N-alpha-acetyltransferase 10, NatA catalytic subunit | Often (30–79%) | In 2 conditions |
| NIPA1NIPA magnesium transporter 1 | Often (30–79%) | In 1 condition |
| NIPA2NIPA magnesium transporter 2 | Often (30–79%) | In 1 condition |
| NSD2nuclear receptor binding SET domain protein 2 | Often (30–79%) | In 1 condition |
| PLCB4phospholipase C beta 4 | Often (30–79%) | In 1 condition |
| RNF2ring finger protein 2 | Often (30–79%) | In 1 condition |
| SIX1SIX homeobox 1 | Often (30–79%) | In 1 condition |
| SIX5SIX homeobox 5 | Often (30–79%) | In 1 condition |
| TBX15T-box transcription factor 15 | Often (30–79%) | In 1 condition |
| TRAPPC9trafficking protein particle complex subunit 9 | Often (30–79%) | In 1 condition |
| TUBG1tubulin gamma 1 | Often (30–79%) | In 1 condition |
| TWIST1twist family bHLH transcription factor 1 | Often (30–79%) | In 1 condition |
| VAC14VAC14 component of PIKFYVE complex | Often (30–79%) | In 1 condition |
| WFS1wolframin ER transmembrane glycoprotein | Often (30–79%) | In 1 condition |
| ALG12ALG12 alpha-1,6-mannosyltransferase | Sometimes (5–29%) | In 2 conditions |
| BLNKB cell linker | 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 |
| CD79ACD79a molecule | Sometimes (5–29%) | In 1 condition |
| CD79BCD79b molecule | Sometimes (5–29%) | In 1 condition |
| CHN1chimerin 1 | Sometimes (5–29%) | In 1 condition |
| CNOT1CCR4-NOT transcription complex subunit 1 | Sometimes (5–29%) | In 1 condition |
| COLEC10collectin subfamily member 10 | Sometimes (5–29%) | In 2 conditions |
| COLEC11collectin subfamily member 11 | Sometimes (5–29%) | In 1 condition |
| CTHcystathionine gamma-lyase | Sometimes (5–29%) | In 1 condition |
| DSPdesmoplakin | Sometimes (5–29%) | In 1 condition |
| EMC1ER membrane protein complex subunit 1 | Sometimes (5–29%) | In 1 condition |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Sometimes (5–29%) | In 1 condition |
| ERLIN2ER lipid raft associated 2 | Sometimes (5–29%) | In 2 conditions |
| FAAP100FA core complex associated protein 100 | Sometimes (5–29%) | In 1 condition |
| FAM20CFAM20C golgi associated secretory pathway kinase | 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 |
| FRMPD4FERM and PDZ domain containing 4 | Sometimes (5–29%) | In 1 condition |
| IGHMimmunoglobulin heavy constant mu | Sometimes (5–29%) | In 1 condition |
| IGLL1immunoglobulin lambda like polypeptide 1 | Sometimes (5–29%) | In 1 condition |
| JUPjunction plakoglobin | Sometimes (5–29%) | In 1 condition |
| LMX1BLIM homeobox transcription factor 1 beta | Sometimes (5–29%) | In 1 condition |
| LRRC8Aleucine rich repeat containing 8 VRAC subunit A | 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 |
| MAP3K7mitogen-activated protein kinase kinase kinase 7 | Sometimes (5–29%) | In 1 condition |
| MAPRE2microtubule associated protein RP/EB family member 2 | Sometimes (5–29%) | In 1 condition |
| MASP1MBL associated serine protease 1 | Sometimes (5–29%) | In 1 condition |
| PALB2partner and localizer of BRCA2 | Sometimes (5–29%) | In 1 condition |
| PIK3CDphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta | Sometimes (5–29%) | In 1 condition |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sometimes (5–29%) | In 1 condition |
| PMM2phosphomannomutase 2 | Sometimes (5–29%) | In 1 condition |
| PORcytochrome p450 oxidoreductase | 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 |
| RAI1retinoic acid induced 1 | Sometimes (5–29%) | In 1 condition |
| RBMXRNA binding motif protein X-linked | Sometimes (5–29%) | In 1 condition |
| RFWD3ring finger and WD repeat domain 3 | Sometimes (5–29%) | In 1 condition |
| SALL4spalt like transcription factor 4 | Sometimes (5–29%) | In 1 condition |
| SLC26A2solute carrier family 26 member 2 | Sometimes (5–29%) | In 1 condition |
| SLX4SLX4 structure-specific endonuclease subunit | Sometimes (5–29%) | In 1 condition |
| SMARCD2SWI/SNF related BAF chromatin remodeling complex subunit D2 | Sometimes (5–29%) | In 1 condition |
| SPI1Spi-1 proto-oncogene | Sometimes (5–29%) | In 1 condition |
| STXBP1syntaxin binding protein 1 | Sometimes (5–29%) | In 1 condition |
| TCF3transcription factor 3 | Sometimes (5–29%) | In 1 condition |
| TP63tumor protein p63 | Sometimes (5–29%) | In 1 condition |
| TUBBtubulin beta class I | Sometimes (5–29%) | In 1 condition |
| TWIST2twist family bHLH transcription factor 2 | Sometimes (5–29%) | In 1 condition |
| UBE2Tubiquitin conjugating enzyme E2 T | Sometimes (5–29%) | In 1 condition |
| XRCC2X-ray repair cross complementing 2 | Sometimes (5–29%) | In 1 condition |
| EBPEBP cholestenol delta-isomerase | Rarely (1–4%) | In 2 conditions |
| PLOD1procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 | Rarely (1–4%) | In 1 condition |
| SMCHD1structural maintenance of chromosomes flexible hinge domain containing 1 | Rarely (1–4%) | In 1 condition |
| ACTG1actin gamma 1 | Not recorded | In 1 condition |
| AMPD2adenosine monophosphate deaminase 2 | Not recorded | In 1 condition |
| ATRATR checkpoint kinase | Not recorded | In 1 condition |
| B9D2B9 domain containing 2 | Not recorded | In 1 condition |
| BICD2BICD cargo adaptor 2 | Not recorded | In 1 condition |
| CDK10cyclin dependent kinase 10 | Not recorded | In 1 condition |
| COL11A1collagen type XI alpha 1 chain | Not recorded | In 1 condition |
| CUL4Bcullin 4B | Not recorded | In 1 condition |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Not recorded | In 1 condition |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Not recorded | In 1 condition |
| ETFAelectron transfer flavoprotein subunit alpha | Not recorded | In 1 condition |
| ETFBelectron transfer flavoprotein subunit beta | Not recorded | In 1 condition |
| ETFDHelectron transfer flavoprotein dehydrogenase | Not recorded | In 1 condition |
| INTUinturned planar cell polarity protein | Not recorded | In 1 condition |
| KDM5Blysine demethylase 5B | Not recorded | In 1 condition |
| MEOX1mesenchyme homeobox 1 | Not recorded | In 1 condition |
| ORC4origin recognition complex subunit 4 | Not recorded | In 1 condition |
| OTUD6BOTU deubiquitinase 6B | Not recorded | In 1 condition |
| PBX1PBX homeobox 1 | Not recorded | In 1 condition |
| PIEZO1piezo type mechanosensitive ion channel component 1 (Er blood group) | Not recorded | In 1 condition |
| PIGBphosphatidylinositol glycan anchor biosynthesis class B | Not recorded | In 1 condition |
| PTF1Apancreas associated transcription factor 1a | Not recorded | In 1 condition |
| RAB23RAB23, member RAS oncogene family | Not recorded | In 1 condition |
| SKISKI proto-oncogene | Not recorded | In 1 condition |
| SMSspermine synthase | Not recorded | In 1 condition |
| UBE3Bubiquitin protein ligase E3B | Not recorded | In 1 condition |
| WACWW domain containing adaptor with coiled-coil | Not recorded | In 1 condition |
| WNT7AWnt family member 7A | Not recorded | In 1 condition |
| ZBTB18zinc finger and BTB domain containing 18 | 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
- Large ears280 genes
- Prominent ear226 genes
- Cupped ear79 genes
- Simple ear32 genes
- Abnormal earlobe29 genes
- Abnormal helix morphology26 genes
- Abnormal antihelix morphology15 genes
- Thickened ears11 genes
- Lop ear9 genes
- Long ear7 genes
- Round ear7 genes
- Crumpled ear6 genes
- Abnormal tragus morphology4 genes
- Absent/small external ear4 genes
- Calcification of the auricular cartilage4 genes
- Question mark ear4 genes
- Abnormal antitragus morphology3 genes
- Short ear3 genes
- Satyr ear2 genes
- Auricular pit1 gene
- Auricular tag1 gene
- Chondritis of pinna1 gene
- Cystic lesions of the pinnae1 gene
- Deformed external ear on one side1 gene
- Extra concha fold1 gene
- Hypertrophic auricular cartilage1 gene
- Abnormal external ear cartilage morphology
- Abnormal location of ears
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 2026.10.18-8b139e39.
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