Atlas우리가 돕는 분들과학적 근거제품연구 성과
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형질
Double ureter
임상 명칭: Ureteral duplication
A developmental anomaly characterized by the presence of two, instead of one, ureter connecting a kidney to the bladder.
Atlas우리가 돕는 분들과학적 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/ureteral-duplication.json"
page <- fromJSON(url)
page$trait$nameDouble ureterHP:0000073
Atlas우리가 돕는 분들과학적 근거제품연구 성과
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39 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.
- Meckel SyndromeReads 9 of these genesB9D1B9D2MKS1RPGRIP1LTCTN2TMEM107About this report →
- Joubert Syndrome And Related DisordersReads 15 of these genesB9D1B9D2CC2D2ACEP290CSPP1MKS1About this report →
- Kabuki SyndromeReads 2 of these genesKDM6AKMT2DAbout this report →
- Autosomal Recessive Cerebellar Ataxias (incl. CANVAS and AVED)Reads 8 of these genesCC2D2ACEP290CSPP1MKS1TMEM216TMEM231About this report →
Show 35 more reports
- CEP290-Related CiliopathyReads 1 of these genesCEP290About this report →
- Focal Dermal Hypoplasia (Goltz Syndrome)Reads 1 of these genesPORCNAbout this report →
- IFT140-Related CiliopathyReads 1 of these genesIFT140About this report →
- Restrictive Dermopathy (ZMPSTE24)Reads 1 of these genesZMPSTE24About this report →
- Scalp-Ear-Nipple SyndromeReads 1 of these genesKCTD1About this report →
- Simpson-Golabi-Behmel SyndromeReads 1 of these genesGPC3About this report →
- Stankiewicz-Isidor SyndromeReads 1 of these genesPSMD12About this report →
- Hereditary Gingival FibromatosisReads 1 of these genesSOS1About this report →
- LipodystrophyReads 2 of these genesLMNAZMPSTE24About this report →
- Overgrowth Syndromes (Sotos, Weaver, Tatton-Brown-Rahman, Malan)Reads 1 of these genesNSD1About this report →
- Leber Congenital Amaurosis & RPE65-Related RetinopathyReads 2 of these genesCEP290RPGRIP1About this report →
- Bardet-Biedl and Alström SyndromesReads 2 of these genesCEP290MKS1About this report →
- Inherited Neurodegenerative DisordersReads 8 of these genesCC2D2ACEP290CSPP1MKS1TMEM216TMEM231About this report →
- Progressive Cardiac Conduction Disease & Sick Sinus SyndromeReads 1 of these genesLMNAAbout this report →
- Imprinting Disorders: Prader-Willi, Silver-Russell and Beckwith-WiedemannReads 1 of these genesNSD1About this report →
- Heterotaxy & Laterality DefectsReads 1 of these genesNODALAbout this report →
- Polycystic Kidney DiseaseReads 1 of these genesIFT140About this report →
- Congenital Diarrhoeas & EnteropathiesReads 1 of these genesSPINT2About this report →
- Inherited Congenital Heart DefectsReads 1 of these genesGATA6About this report →
- Complex Cortical Dysplasia and Frontoparietal PolymicrogyriaReads 1 of these genesAPC2About this report →
- Hypertrophic CardiomyopathyReads 2 of these genesSOS1NSD1About this report →
- Fatty Acid Oxidation & Carnitine Cycle DisordersReads 1 of these genesCPT2About this report →
- Retinitis PigmentosaReads 2 of these genesIFT140CC2D2AAbout this report →
- GPI Anchor Biosynthesis DefectsReads 1 of these genesPIGNAbout this report →
- Neonatal Diabetes MellitusReads 1 of these genesGATA6About this report →
- Nephronophthisis and Senior-Løken SyndromeReads 1 of these genesTMEM67About this report →
- Noonan SyndromeReads 1 of these genesSOS1About this report →
- Lissencephaly Spectrum DisordersReads 1 of these genesAPC2About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesB3GLCTPIGNAbout this report →
- Diabetes MellitusReads 1 of these genesGATA6About this report →
- Inherited ThrombocytopeniasReads 1 of these genesRBM8AAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesLMNAAbout this report →
- Dilated CardiomyopathyReads 1 of these genesLMNAAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesLMNAAbout this report →
- Rare Hereditary Peripheral NeuropathiesReads 1 of these genesLMNAAbout this report →
연관 유전자 42개: Double ureter
이 유전자들의 변화는 Double ureter 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 |
|---|---|---|
| IFT140intraflagellar transport 140 | 항상 | 질환 1개에서 나타남 |
| FUZfuzzy planar cell polarity protein | 자주 (30–79%) | 질환 1개에서 나타남 |
| GPC3glypican 3 | 자주 (30–79%) | 질환 1개에서 나타남 |
| GPC4glypican 4 | 자주 (30–79%) | 질환 1개에서 나타남 |
| NCAPG2non-SMC condensin II complex subunit G2 | 자주 (30–79%) | 질환 1개에서 나타남 |
| SLC6A17solute carrier family 6 member 17 | 자주 (30–79%) | 질환 2개에서 나타남 |
| VANGL1VANGL planar cell polarity protein 1 | 자주 (30–79%) | 질환 1개에서 나타남 |
| B3GLCTbeta 3-glucosyltransferase | 가끔 (5–29%) | 질환 2개에서 나타남 |
| B9D1B9 domain containing 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| B9D2B9 domain containing 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CC2D2Acoiled-coil and C2 domain containing 2A | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CEP290centrosomal protein 290 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| CSPP1centrosome and spindle pole associated protein 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| GATA6GATA binding protein 6 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| KCTD1potassium channel tetramerization domain containing 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| KDM6Alysine demethylase 6A | 가끔 (5–29%) | 질환 1개에서 나타남 |
| KMT2Dlysine methyltransferase 2D | 가끔 (5–29%) | 질환 1개에서 나타남 |
| LMNAlamin A/C | 가끔 (5–29%) | 질환 1개에서 나타남 |
| MKS1MKS transition zone complex subunit 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| PSMD12proteasome 26S subunit, non-ATPase 12 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| RPGRIP1RPGR interacting protein 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| RPGRIP1LRPGRIP1 like | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SOS1SOS Ras/Rac guanine nucleotide exchange factor 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| SPINT2serine peptidase inhibitor, Kunitz type 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TCTN1tectonic family member 1 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TCTN2tectonic family member 2 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TCTN3tectonic family member 3 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TMEM107transmembrane protein 107 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TMEM216transmembrane protein 216 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TMEM231transmembrane protein 231 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TMEM237transmembrane protein 237 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TMEM67transmembrane protein 67 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| TXNDC15thioredoxin domain containing 15 | 가끔 (5–29%) | 질환 1개에서 나타남 |
| ZMPSTE24zinc metallopeptidase STE24 | 가끔 (5–29%) | 질환 2개에서 나타남 |
| APC2APC regulator of Wnt signaling pathway 2 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| NODALnodal growth differentiation factor | 드물게 (1–4%) | 질환 1개에서 나타남 |
| NSD1nuclear receptor binding SET domain protein 1 | 드물게 (1–4%) | 질환 1개에서 나타남 |
| RBM8ARNA binding motif protein 8A | 드물게 (1–4%) | 질환 1개에서 나타남 |
| AXIN1axin 1 | 기록되지 않음 | 질환 1개에서 나타남 |
| CPT2carnitine palmitoyltransferase 2 | 기록되지 않음 | 질환 1개에서 나타남 |
유전자 2개 더 보기
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.
Atlas우리가 돕는 분들과학적 근거제품연구 성과
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