Atlas이런 분들을 위해과학적 근거제품연구 성과
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형질
Pancreatic inflammation
임상 명칭: Pancreatitis
The presence of inflammation in the pancreas.
Atlas이런 분들을 위해과학적 근거제품연구 성과
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이 페이지의 데이터
페이지 주소 끝에 .json을 붙이거나 application/json을 요청하면 JSON 형식으로 읽을 수 있습니다.
library(jsonlite)
url <- "https://dantelabs.com/traits/pancreatitis.json"
page <- fromJSON(url)
page$trait$namePancreatic inflammationHP:0001733
Atlas이런 분들을 위해과학적 근거제품연구 성과
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Pancreatic inflammation과(와) 연결된 유전자와 나머지 게놈을 한 번의 검사로 확인하세요.
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내 Genome Test 받기56 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.
- Inherited Parathyroid & Calcium-Sensing DisordersReads 4 of these genesCDC73AP2S1CASRGNA11About this report →
- PancreatitisReads 3 of these genesCTRCPRSS1SPINK1About this report →
- Autoimmune Polyendocrine Syndrome Type 1 (APECED)Reads 1 of these genesAIREAbout this report →
- Cystic FibrosisReads 1 of these genesCFTRAbout this report →
Show 52 more reports
- Familial Mediterranean FeverReads 1 of these genesMEFVAbout this report →
- Low phospholipid-associated cholelithiasisReads 1 of these genesABCB4About this report →
- Wilson DiseaseReads 1 of these genesATP7BAbout this report →
- Thyroid CancerReads 5 of these genesAIRECDC73GNASCASRGNA11About this report →
- Inflammatory Bowel Diseases (IBD)Reads 2 of these genesIL10TGFB1About this report →
- Methylmalonic & Propionic AcidemiaReads 3 of these genesMMUTPCCAPCCBAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 2 of these genesCTLA4FASAbout this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 3 of these genesETFAETFBETFDHAbout this report →
- CitrullinemiaReads 1 of these genesSLC25A13About this report →
- Fibrodysplasia Ossificans ProgressivaReads 1 of these genesGNASAbout this report →
- Autoimmune DiseaseReads 3 of these genesAIRECTLA4FASAbout this report →
- Familial Intrahepatic CholestasisReads 2 of these genesABCB4ATP8B1About this report →
- Mendelian Susceptibility to Mycobacterial Disease (MSMD)Reads 2 of these genesIFNGR1IL23RAbout this report →
- LipodystrophyReads 2 of these genesLMNAPPARGAbout this report →
- Urea Cycle DisorderReads 2 of these genesSLC25A13SLC7A7About this report →
- Disorder of Copper MetabolismReads 1 of these genesATP7BAbout this report →
- Immuno-Osseous DysplasiasReads 1 of these genesSMARCAL1About this report →
- Glycogen Storage DiseaseReads 2 of these genesSLC37A4G6PC1About this report →
- Carney Complex & Hereditary Adrenal Cushing SyndromeReads 1 of these genesPDE11AAbout this report →
- Maple Syrup Urine DiseaseReads 1 of these genesBCKDHAAbout this report →
- Pseudohypoparathyroidism & GNAS-Inactivation DisordersReads 1 of these genesGNASAbout this report →
- Other Inborn Errors of ImmunityReads 7 of these genesC4ACTLA4FASIKZF1IL10IL23RAbout this report →
- Sclerosing Bone Dysplasias (High Bone Mass)Reads 1 of these genesTGFB1About this report →
- Bardet-Biedl and Alström SyndromesReads 2 of these genesIFT172ALMS1About this report →
- Hereditary Visceral Myopathy, CIPO & MMIHSReads 1 of these genesACTG2About this report →
- Hypertrophic CardiomyopathyReads 3 of these genesETFAETFBETFDHAbout this report →
- Colorectal Cancer & PolyposisReads 1 of these genesAPCAbout this report →
- IPEX Syndrome and Other TregopathiesReads 1 of these genesCTLA4About this report →
- Malignant Endocrine NeoplasmReads 1 of these genesCDC73About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Common Variable Immunodeficiency (Monogenic CVID)Reads 1 of these genesIKZF1About this report →
- HyperlipidemiaReads 1 of these genesAPOC2About this report →
- Primary Mitochondrial DiseaseReads 3 of these genesNFS1MPV17NDUFS3About this report →
- Inherited Complement and Properdin DeficienciesReads 1 of these genesC4AAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- Charcot-Marie-Tooth DiseaseReads 2 of these genesLMNAMPV17About this report →
- Homocystinuria & Cobalamin DisordersReads 1 of these genesCBSAbout this report →
- Syndromic Complex Neurodevelopmental DisorderReads 1 of these genesPAN2About this report →
- Rare Hereditary Peripheral NeuropathiesReads 3 of these genesLMNAMPV17NDUFS3About this report →
- Inherited ThrombocytopeniasReads 1 of these genesFLI1About this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesSTUB1About this report →
- Male InfertilityReads 1 of these genesCFTRAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 1 of these genesSTUB1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesPNPLA2About this report →
- Leigh SyndromeReads 1 of these genesNDUFS3About this report →
- Other Inherited LeukodystrophiesReads 1 of these genesNADK2About this report →
- Retinitis PigmentosaReads 1 of these genesIFT172About this report →
- Inherited Neurodegenerative DisordersReads 2 of these genesNADK2STUB1About this report →
- Congenital Disorders of GlycosylationReads 1 of these genesSLC37A4About this report →
- Intellectual DisabilityReads 1 of these genesTCF4About this report →
Pancreatic inflammation과(와) 연결된 유전자와 나머지 게놈을 한 번의 검사로 확인하세요.
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내 Genome Test 받기연관 유전자 76개: Pancreatic inflammation
이 유전자들의 변화는 Pancreatic inflammation 증상이 나타나는 희귀 질환을 일으킵니다. 이 형질을 가진 대부분의 사람에게는 이러한 질환이 없으며, 이 목록에 있는 유전자가 누구의 개인 유전체에 대해서도 말해 주는 것은 없습니다.
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| AIREautoimmune regulator | 항상 | 질환 1개에서 나타남 |
| ESAMendothelial cell adhesion molecule | 항상 | 질환 1개에서 나타남 |
| LMF1lipase maturation factor 1 | 항상 | 질환 1개에서 나타남 |
| PAN2poly(A) specific ribonuclease subunit PAN2 | 항상 | 질환 1개에서 나타남 |
| CIDECcell death inducing DFFA like effector c | 매우 자주 (80–99%) | 질환 1개에서 나타남 |
| APOC2apolipoprotein C2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| IFT172intraflagellar transport 172 | 자주 (30–79%) | 질환 1개에서 나타남 |
| NADK2NAD kinase 2, mitochondrial | 자주 (30–79%) | 질환 1개에서 나타남 |
| NFS1NFS1 cysteine desulfurase | 자주 (30–79%) | 질환 1개에서 나타남 |
| SLC37A4solute carrier family 37 member 4 | 자주 (30–79%) | 질환 2개에서 나타남 |
| UQCRHubiquinol-cytochrome c reductase hinge protein | 자주 (30–79%) | 질환 1개에서 나타남 |
| ABCB4ATP binding cassette subfamily B member 4 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| ACTG2actin gamma 2, smooth muscle | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ATP7BATPase copper transporting beta | 가끔 (5–29%) | 질환 1개에서 나타남 |
| C4Acomplement C4A (Chido/Rodgers blood group) | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CBScystathionine beta-synthase | 가끔 (5–29%) | 질환 2개에서 나타남 |
| CCR1C-C motif chemokine receptor 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CDC73cell division cycle 73 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| CFTRCF transmembrane conductance regulator | 가끔 (5–29%) | 질환 2개에서 나타남 |
| CRELD1CRELD disulfide isomerase 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ERAP1endoplasmic reticulum aminopeptidase 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ETFAelectron transfer flavoprotein subunit alpha | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ETFBelectron transfer flavoprotein subunit beta | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ETFDHelectron transfer flavoprotein dehydrogenase | 가끔 (5–29%) | 질환 1개에서 나타남 |
| FASFas cell surface death receptor | 가끔 (5–29%) | 질환 1개에서 나타남 |
| FCGR2AFc gamma receptor IIa | 가끔 (5–29%) | 질환 1개에서 나타남 |
| FLI1Fli-1 proto-oncogene, ETS transcription factor | 가끔 (5–29%) | 질환 1개에서 나타남 |
| GNASGNAS complex locus | 가끔 (5–29%) | 질환 1개에서 나타남 |
| GPR35G protein-coupled receptor 35 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| HLA-Bmajor histocompatibility complex, class I, B | 가끔 (5–29%) | 질환 2개에서 나타남 |
| HLA-DPA1major histocompatibility complex, class II, DP alpha 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| HLA-DPB1major histocompatibility complex, class II, DP beta 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IFNGR1interferon gamma receptor 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IKZF1IKAROS family zinc finger 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IL10interleukin 10 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IL12Ainterleukin 12A | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IL12A-AS1IL12A antisense RNA 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| IL23Rinterleukin 23 receptor | 가끔 (5–29%) | 질환 1개에서 나타남 |
| KLRC4killer cell lectin like receptor C4 | 가끔 (5–29%) | 질환 1개에서 나타남 |
유전자 36개 더 보기
| 유전자 | 나타나는 빈도 | 질환 |
|---|---|---|
| LMNAlamin A/C | 가끔 (5–29%) | 질환 4개에서 나타남 |
| MEFVMEFV innate immunity regulator, pyrin | 가끔 (5–29%) | 질환 2개에서 나타남 |
| MMUTmethylmalonyl-CoA mutase | 가끔 (5–29%) | 질환 3개에서 나타남 |
| MPV17mitochondrial inner membrane protein MPV17 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| MST1macrophage stimulating 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PDE11Aphosphodiesterase 11A | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PNPLA2patatin like domain 2, triacylglycerol lipase | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PPARGperoxisome proliferator activated receptor gamma | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PRTN3proteinase 3 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PTPN22protein tyrosine phosphatase non-receptor type 22 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SEMA4Dsemaphorin 4D | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SLC25A13solute carrier family 25 member 13 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| SLC7A7solute carrier family 7 member 7 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| STAT4signal transducer and activator of transcription 4 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TCF4transcription factor 4 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TGFB1transforming growth factor beta 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TKFCtriokinase and FMN cyclase | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TLR4toll like receptor 4 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| UBAC2UBA domain containing 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ALMS1ALMS1 centrosome and basal body associated protein | 드물게 (1–4%) | 질환 1개에서 나타남 |
| APCAPC regulator of Wnt signaling pathway | 드물게 (1–4%) | 질환 1개에서 나타남 |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| STUB1STIP1 homology and U-box containing protein 1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| AP2S1adaptor related protein complex 2 subunit sigma 1 | 기록되지 않음 | 질환 1개에서 나타남 |
| ATP8B1ATPase phospholipid transporting 8B1 | 기록되지 않음 | 질환 1개에서 나타남 |
| BCKDHAbranched chain keto acid dehydrogenase E1 subunit alpha | 기록되지 않음 | 질환 1개에서 나타남 |
| CASRcalcium sensing receptor | 기록되지 않음 | 질환 1개에서 나타남 |
| CTRCchymotrypsin C | 기록되지 않음 | 질환 1개에서 나타남 |
| G6PC1glucose-6-phosphatase catalytic subunit 1 | 기록되지 않음 | 질환 1개에서 나타남 |
| GNA11G protein subunit alpha 11 | 기록되지 않음 | 질환 1개에서 나타남 |
| NDUFS3NADH:ubiquinone oxidoreductase core subunit S3 | 기록되지 않음 | 질환 1개에서 나타남 |
| PCCApropionyl-CoA carboxylase subunit alpha | 기록되지 않음 | 질환 1개에서 나타남 |
| PCCBpropionyl-CoA carboxylase subunit beta | 기록되지 않음 | 질환 1개에서 나타남 |
| PRSS1serine protease 1 | 기록되지 않음 | 질환 1개에서 나타남 |
| PRSS2serine protease 2 | 기록되지 않음 | 질환 1개에서 나타남 |
| SPINK1serine peptidase inhibitor Kazal type 1 | 기록되지 않음 | 질환 1개에서 나타남 |
Human Phenotype Ontology가 기록한, 해당 유전자와 관련된 질환을 가진 사람들 가운데 이 특징이 나타나는 빈도입니다. 이 페이지는 특징과 그 바탕이 되는 연구를 설명하며, 진단이 아닙니다. 증상에 대해서는 의사나 유전 상담사에게 문의하시기 바랍니다.
하위 형질
상위 형질
출처
- Human Phenotype Ontology, 버전 2026-09-01: 특징, 명칭, 정의 및 이와 연결된 유전자입니다. 자세한 내용은 hpo.jax.org에서 확인하실 수 있습니다.
- 데이터 버전 2026.10.19-9814e911.
Atlas이런 분들을 위해과학적 근거제품연구 성과
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