Træk
Photosensitive skin
Klinisk navn: Cutaneous photosensitivity
An increased sensitivity of the skin to light. Photosensitivity may result in a rash upon exposure to the sun (which is known as photodermatosis). Photosensitivity can be diagnosed by phototests in which light is shone on small areas of skin.
Resumé
- Også kaldet
- Photosensitive skin rashes, Photosensitivity, Sensitivity to sunlight, Skin photosensitivity, Sun sensitivity
- Kropssystem
- Abnormality of the integument
ReferencegenomGRCh38hg38
Positioner på gen- og variantsider følger dette valg i denne browser.
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Bestil min Genome Test120 gener knyttet til Photosensitive skin
Ændringer i disse gener forårsager sjældne tilstande, hvor Photosensitive skin 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 |
|---|---|---|
| CLPXcaseinolytic mitochondrial matrix peptidase chaperone subunit X | Altid | I 1 tilstand |
| DNA2DNA replication helicase/nuclease 2 | Altid | I 1 tilstand |
| ERCC2ERCC excision repair 2, TFIIH core complex helicase subunit | Altid | I 7 tilstande |
| ERCC3ERCC excision repair 3, TFIIH core complex helicase subunit | Altid | I 5 tilstande |
| ERCC4ERCC excision repair 4, endonuclease catalytic subunit | Altid | I 5 tilstande |
| ERCC5ERCC excision repair 5, endonuclease | Altid | I 5 tilstande |
| ERCC6ERCC excision repair 6, chromatin remodeling factor | Altid | I 6 tilstande |
| ERCC8ERCC excision repair 8, CSA ubiquitin ligase complex subunit | Altid | I 4 tilstande |
| FDFT1farnesyl-diphosphate farnesyltransferase 1 | Altid | I 1 tilstand |
| FDXRferredoxin reductase | Altid | I 1 tilstand |
| GABRA1gamma-aminobutyric acid type A receptor subunit alpha1 | Altid | I 1 tilstand |
| GTF2H4general transcription factor IIH subunit 4 | Altid | I 1 tilstand |
| GTF2H5general transcription factor IIH subunit 5 | Altid | I 2 tilstande |
| IKZF2IKAROS family zinc finger 2 | Altid | I 1 tilstand |
| PCNAproliferating cell nuclear antigen | Altid | I 2 tilstande |
| PLD4phospholipase D family member 4 | Altid | I 1 tilstand |
| POLHDNA polymerase eta | Altid | I 2 tilstande |
| PPOXprotoporphyrinogen oxidase | Altid | I 3 tilstande |
| RECQLRecQ like helicase | Altid | I 1 tilstand |
| RNU2-2RNA, U2 small nuclear 2 | Altid | I 1 tilstand |
| SLC6A19solute carrier family 6 member 19 | Altid | I 2 tilstande |
| URODuroporphyrinogen decarboxylase | Altid | I 1 tilstand |
| XPAXPA, DNA damage recognition and repair factor | Altid | I 2 tilstande |
| CLTRNcollectrin, amino acid transport regulator | Meget ofte (80–99 %) | I 1 tilstand |
| CYBAcytochrome b-245 alpha chain | Meget ofte (80–99 %) | I 1 tilstand |
| CYBBcytochrome b-245 beta chain | Meget ofte (80–99 %) | I 1 tilstand |
| CYBC1cytochrome b-245 chaperone 1 | Meget ofte (80–99 %) | I 1 tilstand |
| DDB2damage specific DNA binding protein 2 | Meget ofte (80–99 %) | I 2 tilstande |
| FECHferrochelatase | Meget ofte (80–99 %) | I 1 tilstand |
| FERMT1FERM domain containing kindlin 1 | Meget ofte (80–99 %) | I 2 tilstande |
| GJA1gap junction protein alpha 1 | Meget ofte (80–99 %) | I 1 tilstand |
| GJB3gap junction protein beta 3 | Meget ofte (80–99 %) | I 1 tilstand |
| GJB4gap junction protein beta 4 | Meget ofte (80–99 %) | I 1 tilstand |
| KDSR3-ketodihydrosphingosine reductase | Meget ofte (80–99 %) | I 1 tilstand |
| NCF1neutrophil cytosolic factor 1 | Meget ofte (80–99 %) | I 1 tilstand |
| NCF2neutrophil cytosolic factor 2 | Meget ofte (80–99 %) | I 1 tilstand |
| NCF4neutrophil cytosolic factor 4 | Meget ofte (80–99 %) | I 1 tilstand |
| PEPDpeptidase D | Meget ofte (80–99 %) | I 1 tilstand |
| XPCXPC complex subunit, DNA damage recognition and repair factor | Meget ofte (80–99 %) | I 2 tilstande |
| ABCB6ATP binding cassette subfamily B member 6 (LAN blood group) | Ofte (30–79 %) | I 1 tilstand |
Vis 80 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| BLMBLM RecQ like helicase | Ofte (30–79 %) | I 2 tilstande |
| CARMIL2capping protein regulator and myosin 1 linker 2 | Ofte (30–79 %) | I 1 tilstand |
| COL7A1collagen type VII alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| DHCR77-dehydrocholesterol reductase | Ofte (30–79 %) | I 1 tilstand |
| DNASE1deoxyribonuclease 1 | Ofte (30–79 %) | I 2 tilstande |
| ERCC1ERCC excision repair 1, endonuclease non-catalytic subunit | Ofte (30–79 %) | I 1 tilstand |
| FCGR2AFc gamma receptor IIa | Ofte (30–79 %) | I 1 tilstand |
| FCGR2BFc gamma receptor IIb | Ofte (30–79 %) | I 2 tilstande |
| FDPSfarnesyl diphosphate synthase | Ofte (30–79 %) | I 1 tilstand |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Ofte (30–79 %) | I 1 tilstand |
| KRT1keratin 1 | Ofte (30–79 %) | I 1 tilstand |
| KRT10keratin 10 | Ofte (30–79 %) | I 1 tilstand |
| LIG4DNA ligase 4 | Ofte (30–79 %) | I 2 tilstande |
| LYSTlysosomal trafficking regulator | Ofte (30–79 %) | I 1 tilstand |
| MAGEL2MAGE family member L2 | Ofte (30–79 %) | I 1 tilstand |
| MKRN3makorin ring finger protein 3 | Ofte (30–79 %) | I 1 tilstand |
| MVDmevalonate diphosphate decarboxylase | Ofte (30–79 %) | I 1 tilstand |
| MVKmevalonate kinase | Ofte (30–79 %) | I 2 tilstande |
| NPAP1nuclear pore associated protein 1 | Ofte (30–79 %) | I 1 tilstand |
| PMVKphosphomevalonate kinase | Ofte (30–79 %) | I 1 tilstand |
| PORCNporcupine O-acyltransferase | Ofte (30–79 %) | I 1 tilstand |
| PWAR1Prader Willi/Angelman region RNA 1 | Ofte (30–79 %) | I 1 tilstand |
| PWRN1Prader-Willi region non-protein coding RNA 1 | Ofte (30–79 %) | I 1 tilstand |
| SAMHD1SAM and HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 | Ofte (30–79 %) | I 1 tilstand |
| SLC17A9solute carrier family 17 member 9 | Ofte (30–79 %) | I 1 tilstand |
| SNORD115-1small nucleolar RNA, C/D box 115-1 | Ofte (30–79 %) | I 1 tilstand |
| SNORD116-1small nucleolar RNA, C/D box 116-1 | Ofte (30–79 %) | I 1 tilstand |
| TREX1three prime repair exonuclease 1 | Ofte (30–79 %) | I 2 tilstande |
| AARS1alanyl-tRNA synthetase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| BANK1B cell scaffold protein with ankyrin repeats 1 | Nogle gange (5–29 %) | I 1 tilstand |
| BLKBLK proto-oncogene, Src family tyrosine kinase | Nogle gange (5–29 %) | I 1 tilstand |
| C4Acomplement C4A (Chido/Rodgers blood group) | Nogle gange (5–29 %) | I 2 tilstande |
| C4Bcomplement C4B (Chido/Rodgers blood group) | Nogle gange (5–29 %) | I 1 tilstand |
| CARS1cysteinyl-tRNA synthetase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| CPOXcoproporphyrinogen oxidase | Nogle gange (5–29 %) | I 3 tilstande |
| CR2complement C3d receptor 2 | Nogle gange (5–29 %) | I 1 tilstand |
| CSTBcystatin B | Nogle gange (5–29 %) | I 1 tilstand |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Nogle gange (5–29 %) | I 1 tilstand |
| DBR1debranching RNA lariats 1 | Nogle gange (5–29 %) | I 1 tilstand |
| DDX6DEAD-box helicase 6 | Nogle gange (5–29 %) | I 1 tilstand |
| ETS1ETS proto-oncogene 1, transcription factor | Nogle gange (5–29 %) | I 1 tilstand |
| FCGR3BFc gamma receptor IIIb | Nogle gange (5–29 %) | I 1 tilstand |
| GTF2E2general transcription factor IIE subunit 2 | Nogle gange (5–29 %) | I 1 tilstand |
| HLA-DRB1major histocompatibility complex, class II, DR beta 1 | Nogle gange (5–29 %) | I 1 tilstand |
| IGHG1immunoglobulin heavy constant gamma 1 (G1m marker) | Nogle gange (5–29 %) | I 1 tilstand |
| IL10interleukin 10 | Nogle gange (5–29 %) | I 1 tilstand |
| IRAK1interleukin 1 receptor associated kinase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| IRF5interferon regulatory factor 5 | Nogle gange (5–29 %) | I 1 tilstand |
| ITGAMintegrin subunit alpha M | Nogle gange (5–29 %) | I 1 tilstand |
| JAZF1JAZF zinc finger 1 | Nogle gange (5–29 %) | I 1 tilstand |
| KCTD1potassium channel tetramerization domain containing 1 | Nogle gange (5–29 %) | I 1 tilstand |
| KIAA0319LKIAA0319 like | Nogle gange (5–29 %) | I 1 tilstand |
| KRT14keratin 14 | Nogle gange (5–29 %) | I 1 tilstand |
| KRT5keratin 5 | Nogle gange (5–29 %) | I 1 tilstand |
| MECP2methyl-CpG binding protein 2 | Nogle gange (5–29 %) | I 1 tilstand |
| MPLKIPM-phase specific PLK1 interacting protein | Nogle gange (5–29 %) | I 1 tilstand |
| NBNnibrin | Nogle gange (5–29 %) | I 1 tilstand |
| PDCD1programmed cell death 1 | Nogle gange (5–29 %) | I 1 tilstand |
| PRICKLE1prickle planar cell polarity protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | Nogle gange (5–29 %) | I 1 tilstand |
| PXKPX domain containing serine/threonine kinase like | Nogle gange (5–29 %) | I 1 tilstand |
| RNF113Aring finger protein 113A | Nogle gange (5–29 %) | I 2 tilstande |
| SCARB2scavenger receptor class B member 2 | Nogle gange (5–29 %) | I 1 tilstand |
| SPP1secreted phosphoprotein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| STAT4signal transducer and activator of transcription 4 | Nogle gange (5–29 %) | I 1 tilstand |
| SYNGAP1synaptic Ras GTPase activating protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TARS1threonyl-tRNA synthetase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| TLR7toll like receptor 7 | Nogle gange (5–29 %) | I 1 tilstand |
| TNFAIP3TNF alpha induced protein 3 | Nogle gange (5–29 %) | I 1 tilstand |
| TNFSF4TNF superfamily member 4 | Nogle gange (5–29 %) | I 1 tilstand |
| TNIP1TNFAIP3 interacting protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| UBE2L3ubiquitin conjugating enzyme E2 L3 | Nogle gange (5–29 %) | I 1 tilstand |
| ALAS25'-aminolevulinate synthase 2 | Ikke registreret | I 1 tilstand |
| EPM2AEPM2A glucan phosphatase, laforin | Ikke registreret | I 1 tilstand |
| IFIH1interferon induced with helicase C domain 1 | Ikke registreret | I 1 tilstand |
| RECQL4RecQ like helicase 4 | Ikke registreret | I 1 tilstand |
| RORBRAR related orphan receptor B | Ikke registreret | I 1 tilstand |
| TP63tumor protein p63 | Ikke registreret | I 1 tilstand |
| UROSuroporphyrinogen III synthase | Ikke registreret | I 1 tilstand |
| UVSSAUV stimulated scaffold protein A | 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.
Én test. Svar for hele livet.
Fra 449 $Gratis forsendelse · Resultater på 6–8 uger