Tratto
Can't control feelings
Nome clinico: Emotional lability
Unstable emotional experiences and frequent mood changes; emotions that are easily aroused, intense, and/or disproportionate to events and circumstances.
Riepilogo
- Detto anche
- Emotional instability, Mood lability
- Sistema corporeo
- Abnormality of the nervous system
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Aggiunga .json all'indirizzo della pagina, oppure richieda application/json, per leggerla come JSON.
library(jsonlite)
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page <- fromJSON(url)
page$trait$nameLeggi i geni collegati a Can't control feelings e il resto del tuo genoma con un unico test.
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Ottieni il mio Genome Test103 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.
- Bardet-Biedl and Alström SyndromesReads 22 of these genesARL6BBIP1BBS1BBS10BBS12BBS2About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 21 of these genesANGANXA11CCNFCHCHD10CHMP2BDCTN1About this report →
- Inherited Neurodegenerative DisordersReads 44 of these genesPRNPANGANXA11ARSAATXN2CCNFAbout this report →
- Frontotemporal DementiaReads 7 of these genesCCNFCHCHD10CHMP2BHNRNPA1SQSTM1TBK1About this report →
Show 99 more reports
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 3 of these genesARMC5PDE11APRKAR1AAbout this report →
- Hereditary Episodic AtaxiasReads 3 of these genesCACNA1ASCN2ASLC1A3About this report →
- Cerebral Arteriopathy with Subcortical Infarcts and LeukoencephalopathyReads 2 of these genesNOTCH3HTRA1About this report →
- Metachromatic LeukodystrophyReads 2 of these genesARSAPSAPAbout this report →
- Neurodegeneration with Brain Iron Accumulation (NBIA)Reads 4 of these genesFTLPANK2PLA2G6C19orf12About this report →
- Familial Hemiplegic MigraineReads 2 of these genesATP1A2CACNA1AAbout this report →
- MedulloblastomaReads 2 of these genesSUFUELP1About this report →
- Rhabdoid Tumour and SWI/SNF Tumour PredispositionReads 2 of these genesSMARCB1SMARCE1About this report →
- Intellectual DisabilityReads 17 of these genesDEAF1LAS1LATRXCREBBPEP300ERBB4About this report →
- NeurofibromatosisReads 2 of these genesNF2SMARCB1About this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 2 of these genesGNASPRKAR1AAbout this report →
- 22q11.2 Deletion SyndromeReads 1 of these genesTBX1About this report →
- Amyotrophic Lateral Sclerosis Susceptibility 24 (NEK1)Reads 1 of these genesNEK1About this report →
- ATP1A2-Related Fetal Akinesia with PolymicrogyriaReads 1 of these genesATP1A2About this report →
- BAP1 Tumour Predisposition SyndromeReads 1 of these genesBAP1About this report →
- Björnstad SyndromeReads 1 of these genesBCS1LAbout this report →
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Curry-Jones Syndrome (Mosaic SMO Syndrome)Reads 1 of these genesSMOAbout this report →
- Genetic Prion Disease (incl. Fatal Familial Insomnia)Reads 1 of these genesPRNPAbout this report →
- Hartnup DiseaseReads 1 of these genesSLC6A19About this report →
- KDM1A-Related Neurodevelopmental DisorderReads 1 of these genesKDM1AAbout this report →
- Krabbe DiseaseReads 1 of these genesGALCAbout this report →
- Li-Fraumeni SyndromeReads 1 of these genesTP53About this report →
- OPTN-Related Normal-Tension GlaucomaReads 1 of these genesOPTNAbout this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- SPTBN1-Related Neurodevelopmental DisorderReads 1 of these genesSPTBN1About this report →
- Stankiewicz-Isidor SyndromeReads 1 of these genesPSMD12About this report →
- TrimethylaminuriaReads 1 of these genesFMO3About this report →
- UNC13A-Related Neurodevelopmental DisordersReads 1 of these genesUNC13AAbout this report →
- Distal MyopathiesReads 4 of these genesHNRNPA1LRP12MATR3VCPAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 14 of these genesARSACHCHD10DCTN1FIG4NEFHNTRK1About this report →
- Bartter DiseaseReads 2 of these genesBSNDCLCNKBAbout this report →
- Epilepsy (Full Panel)Reads 12 of these genesEPM2ANHLRC1ATP1A2ATP1A3CACNA1AGABRG2About this report →
- Inherited Parathyroid & Calcium-Sensing DisordersReads 2 of these genesCASRGNA11About this report →
- Monogenic Obesity (Leptin-Melanocortin Pathway)Reads 2 of these genesLEPRCEP19About this report →
- Acrodermatitis EnteropathicaReads 1 of these genesSLC39A4About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesAKT1About this report →
- Familial Isolated Pituitary Adenoma (FIPA / X-LAG)Reads 1 of these genesAIPAbout this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Nevoid Basal Cell Carcinoma (Gorlin) SyndromeReads 1 of these genesSUFUAbout this report →
- Kidney CancerReads 2 of these genesTP53BAP1About this report →
- Joubert Syndrome And Related DisordersReads 4 of these genesCEP290MKS1NPHP1SUFUAbout this report →
- Coffin-Siris SyndromeReads 2 of these genesSMARCB1SMARCE1About this report →
- Urinary and Renal System TumourReads 2 of these genesTP53BAP1About this report →
- Neuroacanthocytosis and Huntington Disease PhenocopiesReads 1 of these genesVPS13AAbout this report →
- Charcot-Marie-Tooth DiseaseReads 5 of these genesDCTN1FIG4NEFHSPG11VCPAbout this report →
- Other Inherited LeukodystrophiesReads 5 of these genesARSAPSAPTREM2GALCEIF2B1About this report →
- Retinitis PigmentosaReads 5 of these genesARL6BBS2CFAP418IFT172TTC8About this report →
- Thyroid CancerReads 3 of these genesCASRGNA11GNASAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 4 of these genesCEP290MKS1RNF168TWNKAbout this report →
- Lysosomal Storage DiseaseReads 4 of these genesARSAPSAPCTSFGALCAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 3 of these genesATXN2ATP1A3CACNA1AAbout this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesTREM2About this report →
- Familial Paget Disease of BoneReads 1 of these genesSQSTM1About this report →
- TubulinopathiesReads 1 of these genesTUBB3About this report →
- Hereditary Spastic ParaplegiaReads 4 of these genesSPG11SPARTB4GALNT1ZFYVE26About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 2 of these genesNPHP1SDCCAG8About this report →
- Alzheimer diseaseReads 1 of these genesTREM2About this report →
- MTOR Pathway Megalencephaly and Overgrowth DisordersReads 1 of these genesPIK3CAAbout this report →
- Hereditary Sensory and Autonomic Neuropathies (incl. Familial Dysautonomia)Reads 2 of these genesNTRK1ELP1About this report →
- Cornelia de Lange SyndromeReads 1 of these genesHDAC8About this report →
- Vanishing White Matter DiseaseReads 1 of these genesEIF2B1About this report →
- Spinal Muscular AtrophyReads 2 of these genesCHCHD10DCTN1About this report →
- Basal Ganglia CalcificationReads 1 of these genesPDGFBAbout this report →
- Congenital Cranial Dysinnervation DisordersReads 1 of these genesTUBB3About this report →
- Inherited Predisposition to Acute Myeloid LeukaemiaReads 1 of these genesTERTAbout this report →
- Familial Glucocorticoid DeficiencyReads 1 of these genesNR3C1About this report →
- GlaucomaReads 1 of these genesOPTNAbout this report →
- Malignant Endocrine NeoplasmReads 1 of these genesTP53About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 2 of these genesATP1A3SLC2A1About this report →
- Complex Neurodevelopmental Disorder With Motor FeaturesReads 1 of these genesCACNA1AAbout this report →
- Familial Pulmonary FibrosisReads 1 of these genesTERTAbout this report →
- Meckel SyndromeReads 1 of these genesMKS1About this report →
- BH4 Deficiency & Monoamine Neurotransmitter DisordersReads 1 of these genesDDCAbout this report →
- Usher SyndromeReads 1 of these genesCDH23About this report →
- Urea Cycle DisorderReads 1 of these genesNAGSAbout this report →
- Hereditary Optic NeuropathyReads 1 of these genesATP1A3About this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesCTSFAbout this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesTUBB3About this report →
- Glycogen Storage DiseaseReads 1 of these genesPGK1About this report →
- Parkinson DiseaseReads 1 of these genesPLA2G6About this report →
- Primary Mitochondrial DiseaseReads 3 of these genesPOLGTWNKBCS1LAbout this report →
- Autosomal Recessive Primary MicrocephalyReads 1 of these genesPDCD6IPAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesEIF2B1About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 1 of these genesCEP290About this report →
- Noonan SyndromeReads 1 of these genesBRAFAbout this report →
- Dyskeratosis CongenitaReads 1 of these genesTERTAbout this report →
- Hereditary Congenital & Juvenile CataractReads 1 of these genesFTLAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesTRAF7About this report →
- Syndromic CraniosynostosisReads 1 of these genesSMOAbout this report →
- Hearing Loss and DeafnessReads 2 of these genesCDH23USP48About this report →
- Non-Acquired Combined Pituitary Hormone DeficiencyReads 1 of these genesSMOAbout this report →
- Diabetes MellitusReads 1 of these genesEIF2B1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesTRIM32About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesLEPRAbout this report →
- Female InfertilityReads 1 of these genesTWNKAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesBRAFAbout this report →
- Other Inborn Errors of ImmunityReads 1 of these genesTBX1About this report →
Leggi i geni collegati a Can't control feelings e il resto del tuo genoma con un unico test.
A partire da 449 $Spedizione gratuita · Risultati in 6–8 settimane
Ottieni il mio Genome Test168 geni collegati a Can't control feelings
Alterazioni in questi geni causano malattie rare in cui si osserva Can't control feelings. La maggior parte delle persone con questo tratto non presenta nessuna di tali condizioni, e un gene di questo elenco non dice nulla sul genoma di nessuno in particolare.
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| DEAF1DEAF1 transcription factor | Sempre | In 3 condizioni |
| LEPRleptin receptor | Sempre | In 2 condizioni |
| LRRC7leucine rich repeat containing 7 | Sempre | In 1 condizione |
| PDCD6IPprogrammed cell death 6 interacting protein | Sempre | In 1 condizione |
| RRP12ribosomal RNA processing 12 homolog | Sempre | In 1 condizione |
| CASRcalcium sensing receptor | Molto spesso (80–99%) | In 1 condizione |
| CLTRNcollectrin, amino acid transport regulator | Molto spesso (80–99%) | In 1 condizione |
| DDCdopa decarboxylase | Molto spesso (80–99%) | In 1 condizione |
| GNA11G protein subunit alpha 11 | Molto spesso (80–99%) | In 1 condizione |
| HDAC8histone deacetylase 8 | Molto spesso (80–99%) | In 1 condizione |
| LAS1LLAS1 like ribosome biogenesis factor | Molto spesso (80–99%) | In 2 condizioni |
| PRNPprion protein (Kanno blood group) | Molto spesso (80–99%) | In 4 condizioni |
| SLC6A19solute carrier family 6 member 19 | Molto spesso (80–99%) | In 2 condizioni |
| ANGangiogenin | Spesso (30–79%) | In 1 condizione |
| ANXA11annexin A11 | Spesso (30–79%) | In 1 condizione |
| ARMC5armadillo repeat containing 5 | Spesso (30–79%) | In 1 condizione |
| ARSAarylsulfatase A | Spesso (30–79%) | In 4 condizioni |
| ATRXATRX chromatin remodeler | Spesso (30–79%) | In 1 condizione |
| ATXN2ataxin 2 | Spesso (30–79%) | In 1 condizione |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Spesso (30–79%) | In 1 condizione |
| CCNFcyclin F | Spesso (30–79%) | In 1 condizione |
| CDH23cadherin related 23 | Spesso (30–79%) | In 1 condizione |
| CFAP410cilia and flagella associated protein 410 | Spesso (30–79%) | In 1 condizione |
| CHCHD10coiled-coil-helix-coiled-coil-helix domain containing 10 | Spesso (30–79%) | In 1 condizione |
| CHMP2Bcharged multivesicular body protein 2B | Spesso (30–79%) | In 1 condizione |
| CREBBPCREB binding lysine acetyltransferase | Spesso (30–79%) | In 2 condizioni |
| DAOD-amino acid oxidase | Spesso (30–79%) | In 1 condizione |
| DCTN1dynactin subunit 1 | Spesso (30–79%) | In 1 condizione |
| EP300EP300 lysine acetyltransferase | Spesso (30–79%) | In 1 condizione |
| EPM2AEPM2A glucan phosphatase, laforin | Spesso (30–79%) | In 1 condizione |
| ERBB4erb-b2 receptor tyrosine kinase 4 | Spesso (30–79%) | In 1 condizione |
| FAM177A1family with sequence similarity 177 member A1 | Spesso (30–79%) | In 1 condizione |
| FIG4FIG4 phosphoinositide 5-phosphatase | Spesso (30–79%) | In 1 condizione |
| FMO3flavin containing dimethylaniline monoxygenase 3 | Spesso (30–79%) | In 1 condizione |
| FTLferritin light chain | Spesso (30–79%) | In 2 condizioni |
| FUSFUS RNA binding protein | Spesso (30–79%) | In 1 condizione |
| GLE1GLE1 RNA export mediator | Spesso (30–79%) | In 1 condizione |
| GLT8D1glycosyltransferase 8 domain containing 1 | Spesso (30–79%) | In 1 condizione |
| GNASGNAS complex locus | Spesso (30–79%) | In 2 condizioni |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Spesso (30–79%) | In 1 condizione |
Mostra altri 128 geni
| Gene | Frequenza di osservazione | Condizioni |
|---|---|---|
| KDM1Alysine demethylase 1A | Spesso (30–79%) | In 1 condizione |
| LRP12LDL receptor related protein 12 | Spesso (30–79%) | In 1 condizione |
| MATR3matrin 3 | Spesso (30–79%) | In 1 condizione |
| MTPAPmitochondrial poly(A) polymerase | Spesso (30–79%) | In 2 condizioni |
| NEFHneurofilament heavy chain | Spesso (30–79%) | In 1 condizione |
| NEK1NIMA related kinase 1 | Spesso (30–79%) | In 1 condizione |
| NHLRC1NHL repeat containing E3 ubiquitin protein ligase 1 | Spesso (30–79%) | In 1 condizione |
| NOTCH3notch receptor 3 | Spesso (30–79%) | In 1 condizione |
| NR3C1nuclear receptor subfamily 3 group C member 1 | Spesso (30–79%) | In 1 condizione |
| NTRK1neurotrophic receptor tyrosine kinase 1 | Spesso (30–79%) | In 1 condizione |
| OPTNoptineurin | Spesso (30–79%) | In 1 condizione |
| PANK2pantothenate kinase 2 | Spesso (30–79%) | In 1 condizione |
| PFN1profilin 1 | Spesso (30–79%) | In 1 condizione |
| PRPHperipherin | Spesso (30–79%) | In 1 condizione |
| PSAPprosaposin | Spesso (30–79%) | In 3 condizioni |
| SLC39A4solute carrier family 39 member 4 | Spesso (30–79%) | In 2 condizioni |
| SLC6A17solute carrier family 6 member 17 | Spesso (30–79%) | In 2 condizioni |
| SNORD118small nucleolar RNA, C/D box 118 | Spesso (30–79%) | In 1 condizione |
| SOD1superoxide dismutase 1 | Spesso (30–79%) | In 1 condizione |
| SPG11SPG11 vesicle trafficking associated, spatacsin | Spesso (30–79%) | In 1 condizione |
| SPTBN1spectrin beta, non-erythrocytic 1 | Spesso (30–79%) | In 1 condizione |
| SQSTM1sequestosome 1 | Spesso (30–79%) | In 1 condizione |
| SRPK3SRSF protein kinase 3 | Spesso (30–79%) | In 1 condizione |
| TAF15TATA-box binding protein associated factor 15 | Spesso (30–79%) | In 1 condizione |
| TARDBPTAR DNA binding protein | Spesso (30–79%) | In 2 condizioni |
| TBK1TANK binding kinase 1 | Spesso (30–79%) | In 1 condizione |
| TP53tumor protein p53 | Spesso (30–79%) | In 1 condizione |
| TREM2triggering receptor expressed on myeloid cells 2 | Spesso (30–79%) | In 1 condizione |
| UBQLN2ubiquilin 2 | Spesso (30–79%) | In 1 condizione |
| UNC13Aunc-13 homolog A | Spesso (30–79%) | In 1 condizione |
| USP48ubiquitin specific peptidase 48 | Spesso (30–79%) | In 1 condizione |
| USP8ubiquitin specific peptidase 8 | Spesso (30–79%) | In 2 condizioni |
| VAPBVAMP associated protein B and C | Spesso (30–79%) | In 1 condizione |
| VCPvalosin containing protein | Spesso (30–79%) | In 2 condizioni |
| ARL6ARF like GTPase 6 | A volte (5–29%) | In 1 condizione |
| ATP1A2ATPase Na+/K+ transporting subunit alpha 2 | A volte (5–29%) | In 1 condizione |
| ATP1A3ATPase Na+/K+ transporting subunit alpha 3 | A volte (5–29%) | In 3 condizioni |
| BBIP1BBSome interacting protein 1 | A volte (5–29%) | In 1 condizione |
| BBS1Bardet-Biedl syndrome 1 | A volte (5–29%) | In 1 condizione |
| BBS10Bardet-Biedl syndrome 10 | A volte (5–29%) | In 1 condizione |
| BBS12Bardet-Biedl syndrome 12 | A volte (5–29%) | In 1 condizione |
| BBS2Bardet-Biedl syndrome 2 | A volte (5–29%) | In 1 condizione |
| BBS4Bardet-Biedl syndrome 4 | A volte (5–29%) | In 1 condizione |
| BBS5Bardet-Biedl syndrome 5 | A volte (5–29%) | In 1 condizione |
| BBS7Bardet-Biedl syndrome 7 | A volte (5–29%) | In 1 condizione |
| BBS9Bardet-Biedl syndrome 9 | A volte (5–29%) | In 1 condizione |
| BPTFbromodomain PHD finger transcription factor | A volte (5–29%) | In 1 condizione |
| BSNDbarttin CLCNK type accessory subunit beta | A volte (5–29%) | In 1 condizione |
| CACNA1Acalcium voltage-gated channel subunit alpha1 A | A volte (5–29%) | In 1 condizione |
| CEP19centrosomal protein 19 | A volte (5–29%) | In 1 condizione |
| CEP290centrosomal protein 290 | A volte (5–29%) | In 1 condizione |
| CFAP418cilia and flagella associated protein 418 | A volte (5–29%) | In 1 condizione |
| CLCNKAchloride voltage-gated channel Ka | A volte (5–29%) | In 1 condizione |
| CLCNKBchloride voltage-gated channel Kb | A volte (5–29%) | In 1 condizione |
| CTSFcathepsin F | A volte (5–29%) | In 1 condizione |
| GABRG2gamma-aminobutyric acid type A receptor subunit gamma2 | A volte (5–29%) | In 1 condizione |
| GALCgalactosylceramidase | A volte (5–29%) | In 1 condizione |
| GRIK2glutamate ionotropic receptor kainate type subunit 2 | A volte (5–29%) | In 1 condizione |
| GRIN2Aglutamate ionotropic receptor NMDA type subunit 2A | A volte (5–29%) | In 2 condizioni |
| HTRA1HtrA serine peptidase 1 | A volte (5–29%) | In 1 condizione |
| IFT172intraflagellar transport 172 | A volte (5–29%) | In 1 condizione |
| IFT27intraflagellar transport 27 | A volte (5–29%) | In 1 condizione |
| IFT74intraflagellar transport 74 | A volte (5–29%) | In 1 condizione |
| LZTFL1leucine zipper transcription factor like 1 | A volte (5–29%) | In 1 condizione |
| MECP2methyl-CpG binding protein 2 | A volte (5–29%) | In 1 condizione |
| MIR17HGmiR-17-92a-1 cluster host gene | A volte (5–29%) | In 1 condizione |
| MKKSMKKS centrosomal shuttling protein | A volte (5–29%) | In 1 condizione |
| MKS1MKS transition zone complex subunit 1 | A volte (5–29%) | In 1 condizione |
| MT-TL2mitochondrially encoded tRNA-Leu (CUN) 2 | A volte (5–29%) | In 1 condizione |
| NAGSN-acetylglutamate synthase | A volte (5–29%) | In 1 condizione |
| NPHP1nephrocystin 1 | A volte (5–29%) | In 1 condizione |
| PLA2G6phospholipase A2 group VI | A volte (5–29%) | In 2 condizioni |
| POLGDNA polymerase gamma, catalytic subunit | A volte (5–29%) | In 2 condizioni |
| PSMD12proteasome 26S subunit, non-ATPase 12 | A volte (5–29%) | In 1 condizione |
| RFX7regulatory factor X7 | A volte (5–29%) | In 1 condizione |
| RHOBTB2Rho related BTB domain containing 2 | A volte (5–29%) | In 1 condizione |
| RNF125ring finger protein 125 | A volte (5–29%) | In 1 condizione |
| RNF168ring finger protein 168 | A volte (5–29%) | In 1 condizione |
| RNU2-2RNA, U2 small nuclear 2 | A volte (5–29%) | In 1 condizione |
| SARDHsarcosine dehydrogenase | A volte (5–29%) | In 1 condizione |
| SATB2SATB homeobox 2 | A volte (5–29%) | In 1 condizione |
| SCAPERS-phase cyclin A associated protein in the ER | A volte (5–29%) | In 1 condizione |
| SCLT1sodium channel and clathrin linker 1 | A volte (5–29%) | In 1 condizione |
| SCN2Asodium voltage-gated channel alpha subunit 2 | A volte (5–29%) | In 1 condizione |
| SDCCAG8SHH signaling and ciliogenesis regulator SDCCAG8 | A volte (5–29%) | In 1 condizione |
| SLC1A3solute carrier family 1 member 3 | A volte (5–29%) | In 1 condizione |
| SLC2A1solute carrier family 2 member 1 | A volte (5–29%) | In 1 condizione |
| SPARTspartin | A volte (5–29%) | In 2 condizioni |
| SRPX2sushi repeat containing protein X-linked 2 | A volte (5–29%) | In 1 condizione |
| TNIKTRAF2 and NCK interacting kinase | A volte (5–29%) | In 1 condizione |
| TRIM32tripartite motif containing 32 | A volte (5–29%) | In 1 condizione |
| TTC8tetratricopeptide repeat domain 8 | A volte (5–29%) | In 1 condizione |
| TUBB3tubulin beta 3 class III | A volte (5–29%) | In 1 condizione |
| TWNKtwinkle mtDNA helicase | A volte (5–29%) | In 1 condizione |
| VPS13Avacuolar protein sorting 13 homolog A | A volte (5–29%) | In 2 condizioni |
| WDPCPWD repeat containing planar cell polarity effector | A volte (5–29%) | In 1 condizione |
| AKT1AKT serine/threonine kinase 1 | Raramente (1–4%) | In 1 condizione |
| BAP1BRCA1 associated deubiquitinase 1 | Raramente (1–4%) | In 1 condizione |
| NF2NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor | Raramente (1–4%) | In 1 condizione |
| PDGFBplatelet derived growth factor subunit B | Raramente (1–4%) | In 1 condizione |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Raramente (1–4%) | In 1 condizione |
| SMARCB1SWI/SNF related BAF chromatin remodeling complex subunit B1 | Raramente (1–4%) | In 1 condizione |
| SMARCE1SWI/SNF related BAF chromatin remodeling complex subunit E1 | Raramente (1–4%) | In 1 condizione |
| SMOsmoothened, frizzled class receptor | Raramente (1–4%) | In 1 condizione |
| SUFUSUFU negative regulator of hedgehog signaling | Raramente (1–4%) | In 1 condizione |
| TERTtelomerase reverse transcriptase | Raramente (1–4%) | In 1 condizione |
| TRAF7TNF receptor associated factor 7 | Raramente (1–4%) | In 1 condizione |
| AIPAHR interacting HSP90 co-chaperone | Non registrato | In 1 condizione |
| B4GALNT1beta-1,4-N-acetyl-galactosaminyltransferase 1 | Non registrato | In 1 condizione |
| BCS1LBCS1 ubiquinol-cytochrome c reductase complex chaperone | Non registrato | In 1 condizione |
| C19orf12chromosome 19 open reading frame 12 | Non registrato | In 1 condizione |
| CUL4Bcullin 4B | Non registrato | In 1 condizione |
| DGCR2DiGeorge syndrome critical region gene 2 | Non registrato | In 1 condizione |
| DGCR6DiGeorge syndrome critical region gene 6 | Non registrato | In 1 condizione |
| DGCR8DGCR8 microprocessor complex subunit | Non registrato | In 1 condizione |
| EIF2B1eukaryotic translation initiation factor 2B subunit alpha | Non registrato | In 1 condizione |
| ELP1elongator acetyltransferase complex subunit 1 | Non registrato | In 1 condizione |
| ESS2ess-2 spliceosome associated protein | Non registrato | In 1 condizione |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Non registrato | In 1 condizione |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Non registrato | In 1 condizione |
| MED12mediator complex subunit 12 | Non registrato | In 1 condizione |
| PDE11Aphosphodiesterase 11A | Non registrato | In 1 condizione |
| PGK1phosphoglycerate kinase 1 | Non registrato | In 1 condizione |
| PRKACAprotein kinase cAMP-activated catalytic subunit alpha | Non registrato | In 1 condizione |
| PRKAR1Aprotein kinase cAMP-dependent type I regulatory subunit alpha | Non registrato | In 1 condizione |
| TBX1T-box transcription factor 1 | Non registrato | In 1 condizione |
| TDO2tryptophan 2,3-dioxygenase | Non registrato | In 1 condizione |
| ZFYVE26zinc finger FYVE-type containing 26 | Non registrato | In 1 condizione |
Con quale frequenza questo tratto si presenta tra le persone con una delle condizioni legate al gene, nella misura più alta riscontrata tra queste, secondo quanto registrato dall'Human Phenotype Ontology. Queste pagine descrivono tratti e la ricerca che li riguarda; non costituiscono una diagnosi, e per i sintomi il medico o il consulente genetico è la persona a cui rivolgersi.
Tratti più generali
Fonte dei dati
- Human Phenotype Ontology, versione 2026-09-01: il tratto, i suoi nomi, la sua definizione e i geni a esso collegati. Per saperne di più visiti hpo.jax.org.
- Versione dei dati 2026.10.19-9814e911.
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