AtlasHvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørSekvenser genomet ditt↗
Egenskap
Joint stiffness
Joint stiffness is a perceived sensation of tightness in a joint or joints when attempting to move them after a period of inactivity. Joint stiffness typically subsides over time.
Sammendrag
- Også kalt
- Stiff joint, Stiff joints
- Kroppssystem
- Abnormality of the musculoskeletal system
AtlasHvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørSekvenser genomet ditt↗
Denne siden som data
Legg til .json etter adressen til siden, eller be om application/json, for å lese den som JSON.
library(jsonlite)
url <- "https://dantelabs.com/traits/joint-stiffness.json"
page <- fromJSON(url)
page$trait$nameJoint stiffnessHP:0001387
AtlasHvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørSekvenser genomet ditt↗
Les genene knyttet til Joint stiffness, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test80 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.
- Cornelia de Lange SyndromeReads 6 of these genesBRD4HDAC8NIPBLRAD21SMC1ASMC3About this report →
- Mucopolysaccharidosis Type III (Sanfilippo Syndrome)Reads 4 of these genesHGSNATGNSNAGLUSGSHAbout this report →
- Lysosomal Storage DiseaseReads 13 of these genesGLB1GNPTGIDUAGNPTABGUSBSUMF1About this report →
- Achondrogenesis panelReads 3 of these genesCOL2A1GDF5SLC26A2About this report →
Show 76 more reports
- Wolfram Syndrome & WFS1 SpectrumReads 2 of these genesCISD2WFS1About this report →
- Epiphyseal and Spondyloepiphyseal DysplasiasReads 4 of these genesCOL2A1SLC26A2COMPMATN3About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 7 of these genesERCC1ERCC2ERCC5RAB18RAB3GAP1RAB3GAP2About this report →
- Mucolipidoses (ML II, ML III and ML IV)Reads 2 of these genesGNPTGGNPTABAbout this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 2 of these genesEZH2NSD1About this report →
- AlkaptonuriaReads 1 of these genesHGDAbout this report →
- Canavan DiseaseReads 1 of these genesASPAAbout this report →
- FGFR3-Related Chondrodysplasias (Achondroplasia and Related Conditions)Reads 1 of these genesFGFR3About this report →
- GM1 Gangliosidosis and Morquio B SyndromeReads 1 of these genesGLB1About this report →
- Mucopolysaccharidosis Type I (Hurler and Scheie Syndromes)Reads 1 of these genesIDUAAbout this report →
- Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome)Reads 1 of these genesARSBAbout this report →
- Mucopolysaccharidosis Type VII (Sly Syndrome)Reads 1 of these genesGUSBAbout this report →
- Primary Failure of Tooth EruptionReads 1 of these genesPTH1RAbout this report →
- Rett Syndrome and MECP2-Related DisordersReads 1 of these genesMECP2About this report →
- SHOX Deficiency (Leri-Weill and Langer Dysplasia)Reads 1 of these genesSHOXAbout this report →
- Werner SyndromeReads 1 of these genesWRNAbout this report →
- Marfan Like SyndromesReads 3 of these genesFBN1FBN2SKIAbout this report →
- LipodystrophyReads 3 of these genesLMNAMFN2ZMPSTE24About this report →
- Inherited Congenital Heart DefectsReads 3 of these genesTBX5ELNFLNAAbout this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 2 of these genesACTG2FLNAAbout this report →
- Alpha-Mannosidosis and Other GlycoproteinosesReads 2 of these genesAGAMAN2B1About this report →
- IPEX Syndrome and Other TregopathiesReads 2 of these genesIL2RAIL2RBAbout this report →
- Dilated CardiomyopathyReads 5 of these genesLMNAEMDFHL1SYNE1PRDM16About this report →
- Cowden Syndrome (PTEN hamartoma tumour syndrome)Reads 1 of these genesAKT1About this report →
- Dent Disease and Lowe SyndromeReads 1 of these genesOCRLAbout this report →
- Hereditary FibromatosesReads 1 of these genesANTXR2About this report →
- Inherited ArthropathiesReads 1 of these genesANKHAbout this report →
- Juvenile Polyposis SyndromeReads 1 of these genesSMAD4About this report →
- DNA Repair DiseaseReads 4 of these genesERCC1ERCC2ERCC5ERCC6About this report →
- Immuno-Osseous DysplasiasReads 1 of these genesRNU4ATACAbout this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 3 of these genesACTBPNKDPRRT2About this report →
- Hereditary Hypotrichosis, Woolly Hair and MonilethrixReads 2 of these genesKRT83LSSAbout this report →
- Familial Paget Disease of BoneReads 1 of these genesTNFRSF11BAbout this report →
- Hereditary Hemorrhagic TelangiectasiaReads 1 of these genesSMAD4About this report →
- Molybdenum Cofactor & Isolated Sulfite Oxidase DeficiencyReads 1 of these genesGPHNAbout this report →
- Charcot-Marie-Tooth DiseaseReads 4 of these genesLMNAMFN2TRPV4NAGLUAbout this report →
- Neonatal Diabetes MellitusReads 2 of these genesIL2RAPTF1AAbout this report →
- Hereditary Congenital & Juvenile CataractReads 2 of these genesLSSWFS1About this report →
- Syndromic CraniosynostosisReads 2 of these genesFGFR3SKIAbout this report →
- Other Inborn Errors of ImmunityReads 6 of these genesCD247IL2RAIL2RBNCF1CIITAIL10About this report →
- Chronic Granulomatous DiseaseReads 1 of these genesNCF1About this report →
- HemochromatosisReads 1 of these genesHFEAbout this report →
- Hereditary Orofacial CleftingReads 1 of these genesIRF6About this report →
- Inflammatory Bowel Diseases (IBD)Reads 1 of these genesIL10About this report →
- Waardenburg SyndromeReads 1 of these genesPAX3About this report →
- Diabetes MellitusReads 2 of these genesIL2RAPTF1AAbout this report →
- Severe Combined ImmunodeficiencyReads 2 of these genesCD247CIITAAbout this report →
- GlaucomaReads 1 of these genesLTBP2About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Osteogenesis ImperfectaReads 2 of these genesFKBP10PLOD2About this report →
- Rare Monogenic Autoinflammatory DiseasesReads 2 of these genesPTPN2STING1About this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- Intellectual DisabilityReads 5 of these genesSMAD4BRD4ATRXMECP2RAI1About this report →
- Arrhythmogenic CardiomyopathyReads 1 of these genesTMEM43About this report →
- Epilepsy (Full Panel)Reads 4 of these genesSMC1AMECP2PRRT2FLNAAbout this report →
- Type I InterferonopathiesReads 1 of these genesSTING1About this report →
- Aortic AneurysmReads 1 of these genesFBN1About this report →
- Cutis LaxaReads 1 of these genesELNAbout this report →
- 46,XY Differences of Sex Development and Gonadal DysgenesisReads 1 of these genesATRXAbout this report →
- Congenital MyopathiesReads 1 of these genesTPM2About this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesCBSAbout this report →
- Hearing Loss and DeafnessReads 2 of these genesACTG1WFS1About this report →
- VitreoretinopathyReads 1 of these genesCOL2A1About this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 1 of these genesVAPBAbout this report →
- Congenital Muscular DystrophiesReads 1 of these genesPOMT1About this report →
- Inherited ThrombocytopeniasReads 1 of these genesACTBAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Male InfertilityReads 1 of these genesFKBP6About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesRAB3GAP2About this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesSYNE1About this report →
- Hypertrophic CardiomyopathyReads 1 of these genesNSD1About this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesL1CAMAbout this report →
- Other Inherited LeukodystrophiesReads 1 of these genesASPAAbout this report →
- Retinitis PigmentosaReads 1 of these genesHGSNATAbout this report →
- Congenital Disorders of GlycosylationReads 1 of these genesPOMT1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesDNAJC30About this report →
Les genene knyttet til Joint stiffness, og resten av genomet ditt, med én test.
Fra 449 $Gratis frakt · Resultater på 6–8 uker
Få mitt Genome Test187 gener knyttet til Joint stiffness
Endringer i disse genene forårsaker sjeldne tilstander der Joint stiffness forekommer. De fleste med denne egenskapen har ingen av disse tilstandene, og et gen på denne listen sier ingenting om noens eget genom.
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| ADAMTS10ADAM metallopeptidase with thrombospondin type 1 motif 10 | Alltid | I 2 tilstander |
| ADAMTSL2ADAMTS like 2 | Alltid | I 1 tilstand |
| BANF1barrier to autointegration nuclear assembly factor 1 | Alltid | I 1 tilstand |
| COL2A1collagen type II alpha 1 chain | Alltid | I 4 tilstander |
| GLB1galactosidase beta 1 | Alltid | I 3 tilstander |
| GNPTGN-acetylglucosamine-1-phosphate transferase subunit gamma | Alltid | I 1 tilstand |
| IDUAalpha-L-iduronidase | Alltid | I 3 tilstander |
| KRT83keratin 83 | Alltid | I 1 tilstand |
| LMNAlamin A/C | Alltid | I 4 tilstander |
| SMAD4SMAD family member 4 | Alltid | I 2 tilstander |
| UBAP2Lubiquitin associated protein 2 like | Alltid | I 1 tilstand |
| ADAMTSL4ADAMTS like 4 | Svært ofte (80–99 %) | I 1 tilstand |
| ANTXR2ANTXR cell adhesion molecule 2 | Svært ofte (80–99 %) | I 2 tilstander |
| ATAD1ATPase family AAA domain containing 1 | Svært ofte (80–99 %) | I 1 tilstand |
| BMPR1Bbone morphogenetic protein receptor type 1B | Svært ofte (80–99 %) | I 1 tilstand |
| EMDemerin | Svært ofte (80–99 %) | I 1 tilstand |
| EMG1EMG1 N1-specific pseudouridine methyltransferase | Svært ofte (80–99 %) | I 1 tilstand |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Svært ofte (80–99 %) | I 1 tilstand |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Svært ofte (80–99 %) | I 1 tilstand |
| ERCC5ERCC excision repair 5, endonuclease | Svært ofte (80–99 %) | I 1 tilstand |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Svært ofte (80–99 %) | I 1 tilstand |
| FBN1fibrillin 1 | Svært ofte (80–99 %) | I 6 tilstander |
| FBN2fibrillin 2 | Svært ofte (80–99 %) | I 1 tilstand |
| FGF9fibroblast growth factor 9 | Svært ofte (80–99 %) | I 1 tilstand |
| FHL1four and a half LIM domains 1 | Svært ofte (80–99 %) | I 1 tilstand |
| FKBP10FKBP prolyl isomerase 10 | Svært ofte (80–99 %) | I 2 tilstander |
| GDF5growth differentiation factor 5 | Svært ofte (80–99 %) | I 3 tilstander |
| GDF6growth differentiation factor 6 | Svært ofte (80–99 %) | I 1 tilstand |
| GLRA1glycine receptor alpha 1 | Svært ofte (80–99 %) | I 1 tilstand |
| GLRBglycine receptor beta | Svært ofte (80–99 %) | I 1 tilstand |
| GNPTABN-acetylglucosamine-1-phosphate transferase subunits alpha and beta | Svært ofte (80–99 %) | I 1 tilstand |
| GPHNgephyrin | Svært ofte (80–99 %) | I 1 tilstand |
| HGDhomogentisate 1,2-dioxygenase | Svært ofte (80–99 %) | I 1 tilstand |
| HLA-Bmajor histocompatibility complex, class I, B | Svært ofte (80–99 %) | I 2 tilstander |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Svært ofte (80–99 %) | I 1 tilstand |
| HSPG2heparan sulfate proteoglycan 2 | Svært ofte (80–99 %) | I 2 tilstander |
| IRF6interferon regulatory factor 6 | Svært ofte (80–99 %) | I 1 tilstand |
| LSSlanosterol synthase | Svært ofte (80–99 %) | I 1 tilstand |
| MACROH2A1macroH2A.1 histone | Svært ofte (80–99 %) | I 1 tilstand |
| MFN2mitofusin 2 | Svært ofte (80–99 %) | I 1 tilstand |
Vis 147 gener til
| Gen | Hvor ofte den forekommer | Tilstander |
|---|---|---|
| MMP13matrix metallopeptidase 13 | Svært ofte (80–99 %) | I 1 tilstand |
| MMP9matrix metallopeptidase 9 | Svært ofte (80–99 %) | I 1 tilstand |
| MYH3myosin heavy chain 3 | Svært ofte (80–99 %) | I 3 tilstander |
| NALCNsodium leak channel, non-selective | Svært ofte (80–99 %) | I 3 tilstander |
| NOGnoggin | Svært ofte (80–99 %) | I 1 tilstand |
| P4HA2prolyl 4-hydroxylase subunit alpha 2 | Svært ofte (80–99 %) | I 1 tilstand |
| PAX3paired box 3 | Svært ofte (80–99 %) | I 1 tilstand |
| PIEZO2piezo type mechanosensitive ion channel component 2 | Svært ofte (80–99 %) | I 2 tilstander |
| PITX1paired like homeodomain 1 | Svært ofte (80–99 %) | I 1 tilstand |
| PLOD2procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 | Svært ofte (80–99 %) | I 1 tilstand |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Svært ofte (80–99 %) | I 2 tilstander |
| RAB18RAB18, member RAS oncogene family | Svært ofte (80–99 %) | I 1 tilstand |
| RAB3GAP1RAB3 GTPase activating protein catalytic subunit 1 | Svært ofte (80–99 %) | I 1 tilstand |
| RAB3GAP2RAB3 GTPase activating non-catalytic protein subunit 2 | Svært ofte (80–99 %) | I 1 tilstand |
| SALL4spalt like transcription factor 4 | Svært ofte (80–99 %) | I 1 tilstand |
| SHOXSHOX homeobox | Svært ofte (80–99 %) | I 1 tilstand |
| SLC6A5solute carrier family 6 member 5 | Svært ofte (80–99 %) | I 1 tilstand |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Svært ofte (80–99 %) | I 1 tilstand |
| SYNE2spectrin repeat containing nuclear envelope protein 2 | Svært ofte (80–99 %) | I 1 tilstand |
| TBC1D20TBC1 domain family member 20 | Svært ofte (80–99 %) | I 1 tilstand |
| TBX5T-box transcription factor 5 | Svært ofte (80–99 %) | I 1 tilstand |
| TMEM43transmembrane protein 43 | Svært ofte (80–99 %) | I 1 tilstand |
| TNNI2troponin I2, fast skeletal type | Svært ofte (80–99 %) | I 2 tilstander |
| TNNT3troponin T3, fast skeletal type | Svært ofte (80–99 %) | I 2 tilstander |
| TPM2tropomyosin 2 | Svært ofte (80–99 %) | I 2 tilstander |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Svært ofte (80–99 %) | I 2 tilstander |
| ACTBactin beta | Ofte (30–79 %) | I 1 tilstand |
| ACTG1actin gamma 1 | Ofte (30–79 %) | I 1 tilstand |
| ANKRD55ankyrin repeat domain 55 | Ofte (30–79 %) | I 1 tilstand |
| ASPAaspartoacylase | Ofte (30–79 %) | I 1 tilstand |
| BAZ1Bbromodomain adjacent to zinc finger domain 1B | Ofte (30–79 %) | I 1 tilstand |
| BRD4bromodomain containing 4 | Ofte (30–79 %) | I 1 tilstand |
| BUD23BUD23 rRNA methyltransferase and ribosome maturation factor | Ofte (30–79 %) | I 1 tilstand |
| CBScystathionine beta-synthase | Ofte (30–79 %) | I 1 tilstand |
| CD247CD247 molecule | Ofte (30–79 %) | I 1 tilstand |
| CHST11carbohydrate sulfotransferase 11 | Ofte (30–79 %) | I 1 tilstand |
| CLIP2CAP-Gly domain containing linker protein 2 | Ofte (30–79 %) | I 1 tilstand |
| DNAJC30DnaJ heat shock protein family (Hsp40) member C30 | Ofte (30–79 %) | I 1 tilstand |
| EIF4Heukaryotic translation initiation factor 4H | Ofte (30–79 %) | I 1 tilstand |
| ELNelastin | Ofte (30–79 %) | I 1 tilstand |
| EZH2enhancer of zeste 2 polycomb repressive complex 2 subunit | Ofte (30–79 %) | I 1 tilstand |
| FKBP6FKBP prolyl isomerase family member 6 (inactive) | Ofte (30–79 %) | I 1 tilstand |
| FUZfuzzy planar cell polarity protein | Ofte (30–79 %) | I 1 tilstand |
| GTF2Igeneral transcription factor IIi | Ofte (30–79 %) | I 1 tilstand |
| GTF2IRD1GTF2I repeat domain containing 1 | Ofte (30–79 %) | I 1 tilstand |
| GTF2IRD2GTF2I repeat domain containing 2 | Ofte (30–79 %) | I 1 tilstand |
| GUSBglucuronidase beta | Ofte (30–79 %) | I 2 tilstander |
| HDAC8histone deacetylase 8 | Ofte (30–79 %) | I 1 tilstand |
| HPGD15-hydroxyprostaglandin dehydrogenase | Ofte (30–79 %) | I 1 tilstand |
| IDH1isocitrate dehydrogenase (NADP(+)) 1 | Ofte (30–79 %) | I 1 tilstand |
| IDH2isocitrate dehydrogenase (NADP(+)) 2 | Ofte (30–79 %) | I 1 tilstand |
| IL2RAinterleukin 2 receptor subunit alpha | Ofte (30–79 %) | I 1 tilstand |
| IL2RBinterleukin 2 receptor subunit beta | Ofte (30–79 %) | I 1 tilstand |
| LIMK1LIM domain kinase 1 | Ofte (30–79 %) | I 1 tilstand |
| LTBP2latent transforming growth factor beta binding protein 2 | Ofte (30–79 %) | I 2 tilstander |
| MAU2MAU2 sister chromatid cohesion factor | Ofte (30–79 %) | I 1 tilstand |
| METTL27methyltransferase like 27 | Ofte (30–79 %) | I 1 tilstand |
| MYBPC1myosin binding protein C1 | Ofte (30–79 %) | I 1 tilstand |
| NCF1neutrophil cytosolic factor 1 | Ofte (30–79 %) | I 1 tilstand |
| NIPBLNIPBL cohesin loading factor | Ofte (30–79 %) | I 1 tilstand |
| NPR2natriuretic peptide receptor 2 | Ofte (30–79 %) | I 1 tilstand |
| NSD1nuclear receptor binding SET domain protein 1 | Ofte (30–79 %) | I 1 tilstand |
| POMT1protein O-mannosyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| PTH1Rparathyroid hormone 1 receptor | Ofte (30–79 %) | I 1 tilstand |
| PTPN2protein tyrosine phosphatase non-receptor type 2 | Ofte (30–79 %) | I 1 tilstand |
| RAD21RAD21 cohesin complex component | Ofte (30–79 %) | I 1 tilstand |
| RFC2replication factor C subunit 2 | Ofte (30–79 %) | I 1 tilstand |
| SCUBE3signal peptide, CUB domain and EGF like domain containing 3 | Ofte (30–79 %) | I 1 tilstand |
| SF3B4splicing factor 3b subunit 4 | Ofte (30–79 %) | I 1 tilstand |
| SH3PXD2BSH3 and PX domains 2B | Ofte (30–79 %) | I 1 tilstand |
| SLC26A2solute carrier family 26 member 2 | Ofte (30–79 %) | I 2 tilstander |
| SMC1Astructural maintenance of chromosomes 1A | Ofte (30–79 %) | I 1 tilstand |
| SMC3structural maintenance of chromosomes 3 | Ofte (30–79 %) | I 1 tilstand |
| STAT4signal transducer and activator of transcription 4 | Ofte (30–79 %) | I 1 tilstand |
| STING1stimulator of interferon response cGAMP interactor 1 | Ofte (30–79 %) | I 1 tilstand |
| STX1Asyntaxin 1A | Ofte (30–79 %) | I 1 tilstand |
| SUMF1sulfatase modifying factor 1 | Ofte (30–79 %) | I 1 tilstand |
| SUZ12SUZ12 polycomb repressive complex 2 subunit | Ofte (30–79 %) | I 1 tilstand |
| TBL2transducin beta like 2 | Ofte (30–79 %) | I 1 tilstand |
| TGDSTDP-glucose 4,6-dehydratase | Ofte (30–79 %) | I 1 tilstand |
| TMEM270transmembrane protein 270 | Ofte (30–79 %) | I 1 tilstand |
| USB1U6 snRNA biogenesis phosphodiesterase 1 | Ofte (30–79 %) | I 1 tilstand |
| VANGL1VANGL planar cell polarity protein 1 | Ofte (30–79 %) | I 1 tilstand |
| VPS33AVPS33A core subunit of CORVET and HOPS complexes | Ofte (30–79 %) | I 1 tilstand |
| VPS37DVPS37D subunit of ESCRT-I | Ofte (30–79 %) | I 1 tilstand |
| ACTG2actin gamma 2, smooth muscle | Noen ganger (5–29 %) | I 1 tilstand |
| ADAMTS17ADAM metallopeptidase with thrombospondin type 1 motif 17 | Noen ganger (5–29 %) | I 1 tilstand |
| AGAaspartylglucosaminidase | Noen ganger (5–29 %) | I 1 tilstand |
| AKT1AKT serine/threonine kinase 1 | Noen ganger (5–29 %) | I 1 tilstand |
| ANKHANKH inorganic pyrophosphate transport regulator | Noen ganger (5–29 %) | I 1 tilstand |
| ATRXATRX chromatin remodeler | Noen ganger (5–29 %) | I 1 tilstand |
| BMP6bone morphogenetic protein 6 | Noen ganger (5–29 %) | I 1 tilstand |
| CASZ1castor zinc finger 1 | Noen ganger (5–29 %) | I 1 tilstand |
| CCN2cellular communication network factor 2 | Noen ganger (5–29 %) | I 1 tilstand |
| CHMP1Acharged multivesicular body protein 1A | Noen ganger (5–29 %) | I 1 tilstand |
| CISD2CDGSH iron sulfur domain 2 | Noen ganger (5–29 %) | I 1 tilstand |
| COMPcartilage oligomeric matrix protein | Noen ganger (5–29 %) | I 3 tilstander |
| EPG5ectopic P-granules 5 autophagy tethering factor | Noen ganger (5–29 %) | I 1 tilstand |
| FGFR3fibroblast growth factor receptor 3 | Noen ganger (5–29 %) | I 1 tilstand |
| GABRDgamma-aminobutyric acid type A receptor subunit delta | Noen ganger (5–29 %) | I 1 tilstand |
| HFEhomeostatic iron regulator | Noen ganger (5–29 %) | I 1 tilstand |
| HGSNATheparan-alpha-glucosaminide N-acetyltransferase | Noen ganger (5–29 %) | I 1 tilstand |
| INPPL1inositol polyphosphate phosphatase like 1 | Noen ganger (5–29 %) | I 1 tilstand |
| KCNAB2potassium voltage-gated channel subfamily A regulatory beta subunit 2 | Noen ganger (5–29 %) | I 1 tilstand |
| L1CAML1 cell adhesion molecule | Noen ganger (5–29 %) | I 1 tilstand |
| LEMD3LEM domain containing 3 | Noen ganger (5–29 %) | I 2 tilstander |
| LTBP3latent transforming growth factor beta binding protein 3 | Noen ganger (5–29 %) | I 1 tilstand |
| LUZP1leucine zipper protein 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MAN2B1mannosidase alpha class 2B member 1 | Noen ganger (5–29 %) | I 1 tilstand |
| MATN3matrilin 3 | Noen ganger (5–29 %) | I 1 tilstand |
| MECP2methyl-CpG binding protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| MMP23Bmatrix metallopeptidase 23B | Noen ganger (5–29 %) | I 1 tilstand |
| MTX2metaxin 2 | Noen ganger (5–29 %) | I 1 tilstand |
| NAE1NEDD8 activating enzyme E1 subunit 1 | Noen ganger (5–29 %) | I 1 tilstand |
| OCRLOCRL inositol polyphosphate-5-phosphatase | Noen ganger (5–29 %) | I 1 tilstand |
| PDPNpodoplanin | Noen ganger (5–29 %) | I 1 tilstand |
| PNKDPNKD metallo-beta-lactamase domain containing | Noen ganger (5–29 %) | I 1 tilstand |
| PPP1R12Aprotein phosphatase 1 regulatory subunit 12A | Noen ganger (5–29 %) | I 1 tilstand |
| PRDM16PR/SET domain 16 | Noen ganger (5–29 %) | I 1 tilstand |
| PRKCZprotein kinase C zeta | Noen ganger (5–29 %) | I 1 tilstand |
| PRRT2proline rich transmembrane protein 2 | Noen ganger (5–29 %) | I 1 tilstand |
| RAI1retinoic acid induced 1 | Noen ganger (5–29 %) | I 1 tilstand |
| REREarginine-glutamic acid dipeptide repeats | Noen ganger (5–29 %) | I 1 tilstand |
| RNU4ATACRNA, U4atac small nuclear | Noen ganger (5–29 %) | I 1 tilstand |
| SKISKI proto-oncogene | Noen ganger (5–29 %) | I 2 tilstander |
| SPENspen family transcriptional repressor | Noen ganger (5–29 %) | I 1 tilstand |
| TNFRSF11BTNF receptor superfamily member 11b | Noen ganger (5–29 %) | I 1 tilstand |
| UBE4Bubiquitination factor E4B | Noen ganger (5–29 %) | I 1 tilstand |
| VAPBVAMP associated protein B and C | Noen ganger (5–29 %) | I 1 tilstand |
| WFS1wolframin ER transmembrane glycoprotein | Noen ganger (5–29 %) | I 1 tilstand |
| WRNWRN RecQ like helicase | Noen ganger (5–29 %) | I 1 tilstand |
| ZMPSTE24zinc metallopeptidase STE24 | Noen ganger (5–29 %) | I 1 tilstand |
| FLNAfilamin A | Sjelden (1–4%) | I 1 tilstand |
| PTBP1polypyrimidine tract binding protein 1 | Sjelden (1–4%) | I 1 tilstand |
| ARSBarylsulfatase B | Ikke registrert | I 1 tilstand |
| ASPNasporin | Ikke registrert | I 1 tilstand |
| CCN6cellular communication network factor 6 | Ikke registrert | I 1 tilstand |
| CD244CD244 molecule | Ikke registrert | I 1 tilstand |
| CIITAclass II major histocompatibility complex transactivator | Ikke registrert | I 1 tilstand |
| GNSglucosamine (N-acetyl)-6-sulfatase | Ikke registrert | I 1 tilstand |
| IL10interleukin 10 | Ikke registrert | I 1 tilstand |
| NAGLUN-acetyl-alpha-glucosaminidase | Ikke registrert | I 1 tilstand |
| NFKBIL1NFKB inhibitor like 1 | Ikke registrert | I 1 tilstand |
| PCYT1Aphosphate cytidylyltransferase 1A, choline | Ikke registrert | I 1 tilstand |
| PTF1Apancreas associated transcription factor 1a | Ikke registrert | I 1 tilstand |
| SGSHN-sulfoglucosamine sulfohydrolase | Ikke registrert | I 1 tilstand |
| SLC22A4solute carrier family 22 member 4 | Ikke registrert | I 1 tilstand |
Hvor ofte dette forekommer hos personer med en av genets tilstander, oppgitt som den hyppigste forekomsten blant dem, slik Human Phenotype Ontology registrerer den. Disse sidene beskriver egenskaper og forskningen bak dem. De er ikke en diagnose, og om symptomer bør du spørre lege eller genetisk rådgiver.
Smalere egenskaper
Bredere egenskaper
Slik er informasjonen samlet
- Human Phenotype Ontology, versjon 2026-09-01: egenskapen, navnene på den, definisjonen og genene som er knyttet til den. Les mer på hpo.jax.org.
- Datautgave 2026.10.17-8666dff2.
AtlasHvem vi hjelperVår vitenskapProdukterResultater
Logg innSpørSekvenser genomet ditt↗
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 470+ physician-ready reports.
Fra 449 $
Gratis frakt · Resultater på 6–8 uker
