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Træk
Itching
Klinisk navn: Pruritus
Pruritus is an itch or a sensation that makes a person want to scratch. This term refers to an abnormally increased disposition to experience pruritus.
Resumé
- Også kaldet
- Itchy skin, Skin itching
- Kropssystem
- Abnormality of the integument
ItchingHP:0000989
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Bestil min Genome Test155 gener knyttet til Itching
Ændringer i disse gener forårsager sjældne tilstande, hvor Itching ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| ABCB11ATP binding cassette subfamily B member 11 | Altid | I 4 tilstande |
| ABCB4ATP binding cassette subfamily B member 4 | Altid | I 3 tilstande |
| AMOTL1angiomotin like 1 | Altid | I 1 tilstand |
| ATP8B1ATPase phospholipid transporting 8B1 | Altid | I 5 tilstande |
| CCDC47coiled-coil domain containing 47 | Altid | I 1 tilstand |
| CDSNcorneodesmosin | Altid | I 2 tilstande |
| CLDN1claudin 1 | Altid | I 1 tilstand |
| COL7A1collagen type VII alpha 1 chain | Altid | I 3 tilstande |
| CST3cystatin C | Altid | I 1 tilstand |
| DSG4desmoglein 4 | Altid | I 1 tilstand |
| FLG2filaggrin 2 | Altid | I 1 tilstand |
| MIA3MIA SH3 domain ER export factor 3 | Altid | I 1 tilstand |
| OSMRoncostatin M receptor | Altid | I 1 tilstand |
| PERPp53 apoptosis effector related to PMP22 | Altid | I 1 tilstand |
| PLCG2phospholipase C gamma 2 | Altid | I 1 tilstand |
| PLD4phospholipase D family member 4 | Altid | I 1 tilstand |
| PLECplectin | Altid | I 1 tilstand |
| SLC27A4solute carrier family 27 member 4 | Altid | I 1 tilstand |
| ST14ST14 transmembrane serine protease matriptase | Altid | I 1 tilstand |
| TRPV3transient receptor potential cation channel subfamily V member 3 | Altid | I 1 tilstand |
| USP53ubiquitin specific peptidase 53 | Altid | I 1 tilstand |
| VIPAS39VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog | Altid | I 1 tilstand |
| VPS33BVPS33B late endosome and lysosome associated | Altid | I 1 tilstand |
| ABCA12ATP binding cassette subfamily A member 12 | Meget ofte (80–99 %) | I 2 tilstande |
| ALOX12Barachidonate 12-lipoxygenase, 12R type | Meget ofte (80–99 %) | I 2 tilstande |
| ALOXE3arachidonate epidermal lipoxygenase 3 | Meget ofte (80–99 %) | I 2 tilstande |
| ASPRV1aspartic peptidase retroviral like 1 | Meget ofte (80–99 %) | I 2 tilstande |
| ATP2A2ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2 | Meget ofte (80–99 %) | I 2 tilstande |
| ATP7BATPase copper transporting beta | Meget ofte (80–99 %) | I 1 tilstand |
| CD28CD28 molecule | Meget ofte (80–99 %) | I 2 tilstande |
| CERS3ceramide synthase 3 | Meget ofte (80–99 %) | I 1 tilstand |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Meget ofte (80–99 %) | I 2 tilstande |
| CYP4F22cytochrome P450 family 4 subfamily F member 22 | Meget ofte (80–99 %) | I 1 tilstand |
| DNASE1L3deoxyribonuclease 1L3 | Meget ofte (80–99 %) | I 1 tilstand |
| FECHferrochelatase | Meget ofte (80–99 %) | I 2 tilstande |
| KITKIT proto-oncogene, receptor tyrosine kinase | Meget ofte (80–99 %) | I 3 tilstande |
| KRT14keratin 14 | Meget ofte (80–99 %) | I 3 tilstande |
| KRT5keratin 5 | Meget ofte (80–99 %) | I 5 tilstande |
| LBRlamin B receptor | Meget ofte (80–99 %) | I 2 tilstande |
| LIPNlipase family member N | Meget ofte (80–99 %) | I 1 tilstand |
Vis 115 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| NIPAL4NIPA like domain containing 4 | Meget ofte (80–99 %) | I 2 tilstande |
| NLRP3NLR family pyrin domain containing 3 | Meget ofte (80–99 %) | I 1 tilstand |
| NR1H4nuclear receptor subfamily 1 group H member 4 | Meget ofte (80–99 %) | I 1 tilstand |
| PEPDpeptidase D | Meget ofte (80–99 %) | I 1 tilstand |
| PNPLA1patatin like domain 1, omega-hydroxyceramide transacylase | Meget ofte (80–99 %) | I 1 tilstand |
| SDR9C7short chain dehydrogenase/reductase family 9C member 7 | Meget ofte (80–99 %) | I 2 tilstande |
| SPINK5serine peptidase inhibitor Kazal type 5 | Meget ofte (80–99 %) | I 2 tilstande |
| STAT3signal transducer and activator of transcription 3 | Meget ofte (80–99 %) | I 1 tilstand |
| SULT2B1sulfotransferase family 2B member 1 | Meget ofte (80–99 %) | I 3 tilstande |
| TGM1transglutaminase 1 | Meget ofte (80–99 %) | I 2 tilstande |
| TNFRSF1BTNF receptor superfamily member 1B | Meget ofte (80–99 %) | I 2 tilstande |
| ADAadenosine deaminase | Ofte (30–79 %) | I 1 tilstand |
| ALDH3A2aldehyde dehydrogenase 3 family member A2 | Ofte (30–79 %) | I 1 tilstand |
| AQP5aquaporin 5 | Ofte (30–79 %) | I 1 tilstand |
| ASXL1ASXL transcriptional regulator 1 | Ofte (30–79 %) | I 2 tilstande |
| BRCA1BRCA1 DNA repair associated | Ofte (30–79 %) | I 1 tilstand |
| BRCA2BRCA2 DNA repair associated | Ofte (30–79 %) | I 1 tilstand |
| CARD14caspase recruitment domain family member 14 | Ofte (30–79 %) | I 1 tilstand |
| CBLCbl proto-oncogene | Ofte (30–79 %) | I 1 tilstand |
| CHD7chromodomain helicase DNA binding protein 7 | Ofte (30–79 %) | I 1 tilstand |
| CST6cystatin E/M | Ofte (30–79 %) | I 1 tilstand |
| DCDC2doublecortin domain containing 2 | Ofte (30–79 %) | I 1 tilstand |
| DCLRE1CDNA cross-link repair 1C | Ofte (30–79 %) | I 1 tilstand |
| EPAS1endothelial PAS domain protein 1 | Ofte (30–79 %) | I 1 tilstand |
| EPORerythropoietin receptor | Ofte (30–79 %) | I 1 tilstand |
| FHfumarate hydratase | Ofte (30–79 %) | I 1 tilstand |
| HLA-DQB1major histocompatibility complex, class II, DQ beta 1 | Ofte (30–79 %) | I 1 tilstand |
| HLA-DRAmajor histocompatibility complex, class II, DR alpha | Ofte (30–79 %) | I 1 tilstand |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Ofte (30–79 %) | I 1 tilstand |
| IL12Ainterleukin 12A | Ofte (30–79 %) | I 1 tilstand |
| IL12RB1interleukin 12 receptor subunit beta 1 | Ofte (30–79 %) | I 1 tilstand |
| IL2RGinterleukin 2 receptor subunit gamma | Ofte (30–79 %) | I 1 tilstand |
| IL7Rinterleukin 7 receptor | Ofte (30–79 %) | I 1 tilstand |
| IRF5interferon regulatory factor 5 | Ofte (30–79 %) | I 1 tilstand |
| JAK2Janus kinase 2 | Ofte (30–79 %) | I 2 tilstande |
| KIF12kinesin family member 12 | Ofte (30–79 %) | I 1 tilstand |
| KRT10keratin 10 | Ofte (30–79 %) | I 1 tilstand |
| LRP1LDL receptor related protein 1 | Ofte (30–79 %) | I 2 tilstande |
| MBTPS2membrane bound transcription factor peptidase, site 2 | Ofte (30–79 %) | I 1 tilstand |
| MED12mediator complex subunit 12 | Ofte (30–79 %) | I 1 tilstand |
| MMEL1membrane metalloendopeptidase like 1 | Ofte (30–79 %) | I 1 tilstand |
| MPLMPL proto-oncogene, thrombopoietin receptor | Ofte (30–79 %) | I 1 tilstand |
| MVKmevalonate kinase | Ofte (30–79 %) | I 2 tilstande |
| MYO5Bmyosin VB | Ofte (30–79 %) | I 2 tilstande |
| NUDCD3NudC domain containing 3 | Ofte (30–79 %) | I 1 tilstand |
| PMVKphosphomevalonate kinase | Ofte (30–79 %) | I 1 tilstand |
| PORCNporcupine O-acyltransferase | Ofte (30–79 %) | I 1 tilstand |
| POU2AF1POU class 2 homeobox associating factor 1 | Ofte (30–79 %) | I 1 tilstand |
| PSMB10proteasome 20S subunit beta 10 | Ofte (30–79 %) | I 1 tilstand |
| PTPN3protein tyrosine phosphatase non-receptor type 3 | Ofte (30–79 %) | I 1 tilstand |
| RAG1recombination activating 1 | Ofte (30–79 %) | I 1 tilstand |
| RAG2recombination activating 2 | Ofte (30–79 %) | I 1 tilstand |
| RMRPRNA component of mitochondrial RNA processing endoribonuclease | Ofte (30–79 %) | I 1 tilstand |
| ROS1ROS proto-oncogene 1, receptor tyrosine kinase | Ofte (30–79 %) | I 1 tilstand |
| RUNX1RUNX family transcription factor 1 | Ofte (30–79 %) | I 1 tilstand |
| SAT1spermidine/spermine N1-acetyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| SCN10Asodium voltage-gated channel alpha subunit 10 | Ofte (30–79 %) | I 1 tilstand |
| SCN11Asodium voltage-gated channel alpha subunit 11 | Ofte (30–79 %) | I 2 tilstande |
| SCN9Asodium voltage-gated channel alpha subunit 9 | Ofte (30–79 %) | I 2 tilstande |
| SPIBSpi-B transcription factor | Ofte (30–79 %) | I 1 tilstand |
| SRSF2serine and arginine rich splicing factor 2 | Ofte (30–79 %) | I 2 tilstande |
| STX3syntaxin 3 | Ofte (30–79 %) | I 1 tilstand |
| TET2tet methylcytosine dioxygenase 2 | Ofte (30–79 %) | I 2 tilstande |
| THPOthrombopoietin | Ofte (30–79 %) | I 1 tilstand |
| TNFSF15TNF superfamily member 15 | Ofte (30–79 %) | I 1 tilstand |
| TNPO3transportin 3 | Ofte (30–79 %) | I 1 tilstand |
| UNC45Aunc-45 myosin chaperone A | Ofte (30–79 %) | I 1 tilstand |
| WDR83OSWD repeat domain 83 opposite strand | Ofte (30–79 %) | I 1 tilstand |
| ALKALK receptor tyrosine kinase | Nogle gange (5–29 %) | I 1 tilstand |
| BRAFB-Raf proto-oncogene, serine/threonine kinase | Nogle gange (5–29 %) | I 1 tilstand |
| CASTcalpastatin | Nogle gange (5–29 %) | I 1 tilstand |
| CLEC7AC-type lectin domain containing 7A | Nogle gange (5–29 %) | I 1 tilstand |
| DSPdesmoplakin | Nogle gange (5–29 %) | I 1 tilstand |
| FDPSfarnesyl diphosphate synthase | Nogle gange (5–29 %) | I 1 tilstand |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | Nogle gange (5–29 %) | I 1 tilstand |
| GPNMBglycoprotein nmb | Nogle gange (5–29 %) | I 1 tilstand |
| GPR35G protein-coupled receptor 35 | Nogle gange (5–29 %) | I 1 tilstand |
| GSNgelsolin | Nogle gange (5–29 %) | I 1 tilstand |
| HSD3B7hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7 | Nogle gange (5–29 %) | I 1 tilstand |
| IL17Finterleukin 17F | Nogle gange (5–29 %) | I 1 tilstand |
| IL17RAinterleukin 17 receptor A | Nogle gange (5–29 %) | I 1 tilstand |
| IL17RCinterleukin 17 receptor C | Nogle gange (5–29 %) | I 1 tilstand |
| KRT74keratin 74 | Nogle gange (5–29 %) | I 1 tilstand |
| LIPAlipase A, lysosomal acid type | Nogle gange (5–29 %) | I 1 tilstand |
| MST1macrophage stimulating 1 | Nogle gange (5–29 %) | I 1 tilstand |
| MVDmevalonate diphosphate decarboxylase | Nogle gange (5–29 %) | I 1 tilstand |
| NRASNRAS proto-oncogene, GTPase | Nogle gange (5–29 %) | I 1 tilstand |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Nogle gange (5–29 %) | I 1 tilstand |
| PKP1plakophilin 1 | Nogle gange (5–29 %) | I 1 tilstand |
| POFUT1protein O-fucosyltransferase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| POGLUT1protein O-glucosyltransferase 1 | Nogle gange (5–29 %) | I 2 tilstande |
| PPP1R13Lprotein phosphatase 1 regulatory subunit 13 like | Nogle gange (5–29 %) | I 1 tilstand |
| PSENENpresenilin enhancer, gamma-secretase subunit | Nogle gange (5–29 %) | I 1 tilstand |
| RAF1Raf-1 proto-oncogene, serine/threonine kinase | Nogle gange (5–29 %) | I 1 tilstand |
| SEMA4Dsemaphorin 4D | Nogle gange (5–29 %) | I 1 tilstand |
| SLC17A9solute carrier family 17 member 9 | Nogle gange (5–29 %) | I 1 tilstand |
| SOX5SRY-box transcription factor 5 | Nogle gange (5–29 %) | I 1 tilstand |
| TCF4transcription factor 4 | Nogle gange (5–29 %) | I 1 tilstand |
| TRAF3IP2TRAF3 interacting protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ZEB2zinc finger E-box binding homeobox 2 | Nogle gange (5–29 %) | I 1 tilstand |
| ZFYVE19zinc finger FYVE-type containing 19 | Nogle gange (5–29 %) | I 1 tilstand |
| CTNNB1catenin beta 1 | Sjældent (1–4%) | I 1 tilstand |
| GATA1GATA binding protein 1 | Sjældent (1–4%) | I 1 tilstand |
| LDHAlactate dehydrogenase A | Sjældent (1–4%) | I 1 tilstand |
| URODuroporphyrinogen decarboxylase | Sjældent (1–4%) | I 1 tilstand |
| UROSuroporphyrinogen III synthase | Sjældent (1–4%) | I 1 tilstand |
| IL31RAinterleukin 31 receptor A | Ikke registreret | I 1 tilstand |
| KLK11kallikrein related peptidase 11 | Ikke registreret | I 1 tilstand |
| PDGFRAplatelet derived growth factor receptor alpha | Ikke registreret | I 1 tilstand |
| SLCO1B1solute carrier organic anion transporter family member 1B1 | Ikke registreret | I 1 tilstand |
| SLCO1B3solute carrier organic anion transporter family member 1B3 | Ikke registreret | I 1 tilstand |
| TJP2tight junction protein 2 | Ikke registreret | I 1 tilstand |
| TRPM4transient receptor potential cation channel subfamily M member 4 | Ikke registreret | I 1 tilstand |
| XPNPEP2X-prolyl aminopeptidase 2 | Ikke registreret | I 1 tilstand |
| ZNF341zinc finger protein 341 | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
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Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.16-c6eea6bf.
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