JAG1 c.439+1G>A

Variant ID: 20-10644610-C-T

NM_000214.2(JAG1):c.439+1G>A

This variant was identified in 9 publications

View GRCh38 version.




Publications:


Network expansion of genetic associations defines a pleiotropy map of human cell biology.

Nature Genetics
Barrio-Hernandez, Inigo I; Schwartzentruber, Jeremy J; Shrivastava, Anjali A; Del-Toro, Noemi N; Gonzalez, Asier A; Zhang, Qian Q; Mountjoy, Edward E; Suveges, Daniel D; Ochoa, David D; Ghoussaini, Maya M; Bradley, Glyn G; Hermjakob, Henning H; Orchard, Sandra S; Dunham, Ian I; Anderson, Carl A CA; Porras, Pablo P; Beltrao, Pedro P
Publication Date: 2023-02-23

Variant appearance in text: JAG1: 439+1G>A
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



Different clinical and genetic features of Alagille patients with progressive disease versus a jaundice-free course.

Jgh Open : An Open Access Journal Of Gastroenterology And Hepatology
Chiang, Che-Ming CM; Jeng, Yung-Ming YM; Ho, Ming-Chih MC; Lai, Ming-Wei MW; Li, Huei-Ying HY; Chen, Pei-Lung PL; Lee, Ni-Chung NC; Wu, Jia-Feng JF; Chiu, Yu-Chun YC; Liou, Bang-Yu BY; Ni, Yen-Hsuan YH; Hsu, Hong-Yuan HY; Chang, Mei-Hwei MH; Chen, Huey-Ling HL
Publication Date: 2022-12

Variant appearance in text: JAG1: 439+1G>A; rs863223648
PubMed Link: 36514505
Variant Present in the following documents:
  • Main text
  • JGH3-6-839.pdf
View BVdb publication page



Characterization of the Spectrum of Ophthalmic Changes in Patients With Alagille Syndrome.

Investigative Ophthalmology & Visual Science
da Palma, Mariana Matioli MM; Igelman, Austin D AD; Ku, Cristy C; Burr, Amanda A; You, Jia Yue JY; Place, Emily M EM; Wang, Nan-Kai NK; Oh, Jin Kyun JK; Branham, Kari E KE; Zhang, Xinxin X; Ahn, Jeeyun J; Gorin, Michael B MB; Lam, Byron L BL; Ronquillo, Cecinio C CC; Bernstein, Paul S PS; Nagiel, Aaron A; Huckfeldt, Rachel R; Cabrera, Michelle T MT; Kelly, John P JP; Bakall, Benjamin B; Iannaccone, Alessandro A; Hufnagel, Robert B RB; Zein, Wadih M WM; Koenekoop, Robert K RK; Birch, David G DG; Yang, Paul P; Fahim, Abigail T AT; Pennesi, Mark E ME
Publication Date: 2021-06-01

Variant appearance in text: JAG1: 439+1G>A
PubMed Link: 34185059
Variant Present in the following documents:
  • Main text
  • iovs-62-7-27.pdf
View BVdb publication page



[Clinical characteristics and gene variants of patients with infantile intrahepatic cholestasis].

Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal Of Contemporary Pediatrics
Wang, Mei-Juan MJ; Zhong, Xue-Mei XM; Ma, Xin X; Ning, Hui-Juan HJ; Zhu, Dan D; Gong, You-Zhe YZ; Jin, Meng M
Publication Date: 2021-01

Variant appearance in text: JAG1: 439+1G>A
PubMed Link: 33476544
Variant Present in the following documents:
  • Main text
View BVdb publication page



Alagille syndrome mutation update: Comprehensive overview of JAG1 and NOTCH2 mutation frequencies and insight into missense variant classification.

Human Mutation
Gilbert, Melissa A MA; Bauer, Robert C RC; Rajagopalan, Ramakrishnan R; Grochowski, Christopher M CM; Chao, Grace G; McEldrew, Deborah D; Nassur, James A JA; Rand, Elizabeth B EB; Krock, Bryan L BL; Kamath, Binita M BM; Krantz, Ian D ID; Piccoli, David A DA; Loomes, Kathleen M KM; Spinner, Nancy B NB
Publication Date: 2019-12

Variant appearance in text: JAG1: 439+1G>A
PubMed Link: 31343788
Variant Present in the following documents:
  • HUMU-40-2197.pdf
View BVdb publication page



Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome.

Hypertension (Dallas, Tex. : 1979)
Warejko, Jillian K JK; Schueler, Markus M; Vivante, Asaf A; Tan, Weizhen W; Daga, Ankana A; Lawson, Jennifer A JA; Braun, Daniela A DA; Shril, Shirlee S; Amann, Kassaundra K; Somers, Michael J G MJG; Rodig, Nancy M NM; Baum, Michelle A MA; Daouk, Ghaleb G; Traum, Avram Z AZ; Kim, Heung Bae HB; Vakili, Khashayar K; Porras, Diego D; Lock, James J; Rivkin, Michael J MJ; Chaudry, Gulraiz G; Smoot, Leslie B LB; Singh, Michael N MN; Smith, Edward R ER; Mane, Shrikant M SM; Lifton, Richard P RP; Stein, Deborah R DR; Ferguson, Michael A MA; Hildebrandt, Friedhelm F
Publication Date: 2018-04

Variant appearance in text: JAG1: 439+1G>A
PubMed Link: 29483232
Variant Present in the following documents:
  • Main text
View BVdb publication page



A Landscape of Pharmacogenomic Interactions in Cancer.

Cell
Iorio, Francesco F; Knijnenburg, Theo A TA; Vis, Daniel J DJ; Bignell, Graham R GR; Menden, Michael P MP; Schubert, Michael M; Aben, Nanne N; Gonçalves, Emanuel E; Barthorpe, Syd S; Lightfoot, Howard H; Cokelaer, Thomas T; Greninger, Patricia P; van Dyk, Ewald E; Chang, Han H; de Silva, Heshani H; Heyn, Holger H; Deng, Xianming X; Egan, Regina K RK; Liu, Qingsong Q; Mironenko, Tatiana T; Mitropoulos, Xeni X; Richardson, Laura L; Wang, Jinhua J; Zhang, Tinghu T; Moran, Sebastian S; Sayols, Sergi S; Soleimani, Maryam M; Tamborero, David D; Lopez-Bigas, Nuria N; Ross-Macdonald, Petra P; Esteller, Manel M; Gray, Nathanael S NS; Haber, Daniel A DA; Stratton, Michael R MR; Benes, Cyril H CH; Wessels, Lodewyk F A LFA; Saez-Rodriguez, Julio J; McDermott, Ultan U; Garnett, Mathew J MJ
Publication Date: 2016-07-28

Variant appearance in text: JAG1: 439+1G>A
PubMed Link: 27397505
Variant Present in the following documents:
  • mmc3.xlsx, sheet 2
View BVdb publication page



JAG1 Mutation Spectrum and Origin in Chinese Children with Clinical Features of Alagille Syndrome.

Plos One
Li, Liting L; Dong, Jibin J; Wang, Xiaohong X; Guo, Hongmei H; Wang, Huijun H; Zhao, Jing J; Qiu, Yiling Y; Abuduxikuer, Kuerbanjiang K; Wang, Jianshe J
Publication Date: 2015

Variant appearance in text: JAG1: 439+1G>A
PubMed Link: 26076142
Variant Present in the following documents:
  • Main text
  • pone.0130355.pdf
View BVdb publication page



Spectrum of JAG1 gene mutations in Polish patients with Alagille syndrome.

Journal Of Applied Genetics
Jurkiewicz, Dorota D; Gliwicz, Dorota D; Ciara, Elżbieta E; Gerfen, Jennifer J; Pelc, Magdalena M; Piekutowska-Abramczuk, Dorota D; Kugaudo, Monika M; Chrzanowska, Krystyna K; Spinner, Nancy B NB; Krajewska-Walasek, Małgorzata M
Publication Date: 2014-08

Variant appearance in text: JAG1: 439+1G>A
PubMed Link: 24748328
Variant Present in the following documents:
  • 13353_2014_Article_212.pdf
View BVdb publication page