FURIN c.667+95C>G

Variant ID: 15-91420940-C-G

NM_002569.2(FURIN):c.667+95C>G

This variant was identified in 14 publications

View GRCh38 version.




Publications:


JAK-STAT signaling in inflammatory breast cancer enables chemotherapy-resistant cell states.

Cancer Research
Stevens, Laura E LE; Peluffo, Guillermo G; Qiu, Xintao X; Temko, Daniel D; Fassl, Anne A; Li, Zheqi Z; Trinh, Anne A; Seehawer, Marco M; Jovanovic, Bojana B; Aleckovic, Masa M; Wilde, Callahan M CM; Geck, Renee C RC; Shu, Shaokun S; Kingston, Natalie L NL; Harper, Nicholas W NW; Almendro, Vanessa V; Pyke, Alanna L AL; Egri, Shawn B SB; Papanastasiou, Malvina M; Clement, Kendell K; Zhou, Ningxuan N; Walker, Sarah S; Salas, Jacqueline J; Park, So Yeon SY; Frank, David A DA; Meissner, Alexander A; Jaffe, Jacob D JD; Sicinski, Piotr P; Toker, Alex A; Michor, Franziska F; Long, Henry W HW; Overmoyer, Beth A BA; Polyak, Kornelia K
Publication Date: 2022-11-21

Variant appearance in text: FURIN: 667+95C>G; rs2071410
PubMed Link: 36409824
Variant Present in the following documents:
  • can-22-0423_supplementary_table_s3_suppst3.xlsx, sheet 1
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs2071410
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM15_ESM.xlsx, sheet 2
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A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: rs2071410
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
View BVdb publication page



FURIN Promoter Methylation Predicts the Risk of Incident Diabetes: A Prospective Analysis in the Gusu Cohort.

Frontiers In Endocrinology
He, Yan Y; Li, Yinan Y; Zhang, Jianan J; Chen, Linan L; Li, Jing J; Zhang, Min M; Zhang, Qiu Q; Lu, Ying Y; Jiang, Jun J; Zhang, Xiaolong X; Hu, Jianwei J; Ding, Yi Y; Zhang, Mingzhi M; Peng, Hao H
Publication Date: 2022

Variant appearance in text: rs2071410
PubMed Link: 35399937
Variant Present in the following documents:
  • Main text
  • fendo-13-873012.pdf
View BVdb publication page



ACE2 and FURIN variants are potential predictors of SARS-CoV-2 outcome: A time to implement precision medicine against COVID-19.

Heliyon
Al-Mulla, Fahd F; Mohammad, Anwar A; Al Madhoun, Ashraf A; Haddad, Dania D; Ali, Hamad H; Eaaswarkhanth, Muthukrishnan M; John, Sumi Elsa SE; Nizam, Rasheeba R; Channanath, Arshad A; Abu-Farha, Mohamed M; Ahmad, Rasheed R; Abubaker, Jehad J; Thanaraj, Thangavel Alphonse TA
Publication Date: 2021-02

Variant appearance in text: rs2071410
PubMed Link: 33532652
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Novel germline TRAF3IP3 mutation in a dyad with familial acute B lymphoblastic leukemia.

Cancer Reports (Hoboken, N.J.)
Pommert, Lauren L; Burns, Robert R; Furumo, Quinlan Q; Pulakanti, Kirthi K; Brandt, Jon J; Burke, Michael J MJ; Rao, Sridhar S
Publication Date: 2021-06

Variant appearance in text: FURIN: 667+95C>G; rs2071410
PubMed Link: 33503336
Variant Present in the following documents:
  • CNR2-4-e1335-s003.xlsx, sheet 2
  • CNR2-4-e1335-s003.xlsx, sheet 1
View BVdb publication page



Mouse Models of Human Proprotein Convertase Insufficiency.

Endocrine Reviews
Shakya, Manita M; Lindberg, Iris I
Publication Date: 2021-05-25

Variant appearance in text: rs2071410
PubMed Link: 33382413
Variant Present in the following documents:
  • Main text
View BVdb publication page



FURIN variant associations with postexercise hypotension are intensity and race dependent.

Physiological Reports
Cilhoroz, Burak T BT; Schifano, Elizabeth D ED; Panza, Gregory A GA; Ash, Garrett I GI; Corso, Lauren L; Chen, Ming-Hui MH; Deshpande, Ved V; Zaleski, Amanda A; Farinatti, Paulo P; Santos, Lucas P LP; Taylor, Beth A BA; O'Neill, Rachel J RJ; Thompson, Paul D PD; Pescatello, Linda S LS
Publication Date: 2019-02

Variant appearance in text: rs2071410
PubMed Link: 30706700
Variant Present in the following documents:
  • Main text
  • PHY2-7-e13952.pdf
View BVdb publication page



Pharmacogenomics of the Natriuretic Peptide System in Heart Failure.

Current Heart Failure Reports
Abuzaanona, Ahmed A; Lanfear, David D
Publication Date: 2017-12

Variant appearance in text: rs2071410
PubMed Link: 29075957
Variant Present in the following documents:
  • Main text
View BVdb publication page



Examination of previously identified associations within the Genetic Analysis Workshop 19 data.

Bmc Proceedings
Howey, Richard A J RA; Eu-Ahsunthornwattana, Jakris J; Darlay, Rebecca R; Cordell, Heather J HJ
Publication Date: 2016

Variant appearance in text: rs2071410
PubMed Link: 27980618
Variant Present in the following documents:
  • Main text
  • 12919_2016_Article_12.pdf
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Association of Rs2071410 on Furin with Transient Ischemic Attack Susceptibility and Prognosis in a Chinese Population.

Medical Science Monitor : International Medical Journal Of Experimental And Clinical Research
Sun, Qin-Xiang QX; Zhou, Hai-Mei HM; Du, Qing-Wei QW
Publication Date: 2016-10-19

Variant appearance in text: rs2071410
PubMed Link: 27760099
Variant Present in the following documents:
  • Main text
  • medscimonit-22-3828.pdf
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Genetics of the first seven proprotein convertase enzymes in health and disease.

Current Genomics
Turpeinen, Hannu H; Ortutay, Zsuzsanna Z; Pesu, Marko M
Publication Date: 2013-11

Variant appearance in text: rs2071410
PubMed Link: 24396277
Variant Present in the following documents:
  • Main text
  • CG-14-453.pdf
View BVdb publication page



Loci influencing blood pressure identified using a cardiovascular gene-centric array.

Human Molecular Genetics
Ganesh, Santhi K SK; Tragante, Vinicius V; Guo, Wei W; Guo, Yiran Y; Lanktree, Matthew B MB; Smith, Erin N EN; Johnson, Toby T; Castillo, Berta Almoguera BA; Barnard, John J; Baumert, Jens J; Chang, Yen-Pei Christy YP; Elbers, Clara C CC; Farrall, Martin M; Fischer, Mary E ME; Franceschini, Nora N; Gaunt, Tom R TR; Gho, Johannes M I H JM; Gieger, Christian C; Gong, Yan Y; Isaacs, Aaron A; Kleber, Marcus E ME; Mateo Leach, Irene I; McDonough, Caitrin W CW; Meijs, Matthijs F L MF; Mellander, Olle O; Molony, Cliona M CM; Nolte, Ilja M IM; Padmanabhan, Sandosh S; Price, Tom S TS; Rajagopalan, Ramakrishnan R; Shaffer, Jonathan J; Shah, Sonia S; Shen, Haiqing H; Soranzo, Nicole N; van der Most, Peter J PJ; Van Iperen, Erik P A EP; Van Setten, Jessica J; Van Setten, Jessic A JA; Vonk, Judith M JM; Zhang, Li L; Beitelshees, Amber L AL; Berenson, Gerald S GS; Bhatt, Deepak L DL; Boer, Jolanda M A JM; Boerwinkle, Eric E; Burkley, Ben B; Burt, Amber A; Chakravarti, Aravinda A; Chen, Wei W; Cooper-Dehoff, Rhonda M RM; Curtis, Sean P SP; Dreisbach, Albert A; Duggan, David D; Ehret, Georg B GB; Fabsitz, Richard R RR; Fornage, Myriam M; Fox, Ervin E; Furlong, Clement E CE; Gansevoort, Ron T RT; Hofker, Marten H MH; Hovingh, G Kees GK; Kirkland, Susan A SA; Kottke-Marchant, Kandice K; Kutlar, Abdullah A; Lacroix, Andrea Z AZ; Langaee, Taimour Y TY; Li, Yun R YR; Lin, Honghuang H; Liu, Kiang K; Maiwald, Steffi S; Malik, Rainer R; , ; Murugesan, Gurunathan G; Newton-Cheh, Christopher C; O'Connell, Jeffery R JR; Onland-Moret, N Charlotte NC; Ouwehand, Willem H WH; Palmas, Walter W; Penninx, Brenda W BW; Pepine, Carl J CJ; Pettinger, Mary M; Polak, Joseph F JF; Ramachandran, Vasan S VS; Ranchalis, Jane J; Redline, Susan S; Ridker, Paul M PM; Rose, Lynda M LM; Scharnag, Hubert H; Schork, Nicholas J NJ; Shimbo, Daichi D; Shuldiner, Alan R AR; Srinivasan, Sathanur R SR; Stolk, Ronald P RP; Taylor, Herman A HA; Thorand, Barbara B; Trip, Mieke D MD; van Duijn, Cornelia M CM; Verschuren, W Monique WM; Wijmenga, Cisca C; Winkelmann, Bernhard R BR; Wyatt, Sharon S; Young, J Hunter JH; Boehm, Bernhard O BO; Caulfield, Mark J MJ; Chasman, Daniel I DI; Davidson, Karina W KW; Doevendans, Pieter A PA; Fitzgerald, Garret A GA; Gums, John G JG; Hakonarson, Hakon H; Hillege, Hans L HL; Illig, Thomas T; Jarvik, Gail P GP; Johnson, Julie A JA; Kastelein, John J P JJ; Koenig, Wolfgang W; , ; März, Winfried W; Mitchell, Braxton D BD; Murray, Sarah S SS; Oldehinkel, Albertine J AJ; Rader, Daniel J DJ; Reilly, Muredach P MP; Reiner, Alex P AP; Schadt, Eric E EE; Silverstein, Roy L RL; Snieder, Harold H; Stanton, Alice V AV; Uitterlinden, André G AG; van der Harst, Pim P; van der Schouw, Yvonne T YT; Samani, Nilesh J NJ; Johnson, Andrew D AD; Munroe, Patricia B PB; de Bakker, Paul I W PI; Zhu, Xiaofeng X; Levy, Daniel D; Keating, Brendan J BJ; Asselbergs, Folkert W FW
Publication Date: 2013-04-15

Variant appearance in text: rs2071410
PubMed Link: 23303523
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations between genetic variations in the FURIN gene and hypertension.

Bmc Medical Genetics
Li, Nanfang N; Luo, Wenli W; Juhong, Zhang Z; Yang, Jin J; Wang, Hongmei H; Zhou, Ling L; Chang, Jianhang J
Publication Date: 2010-08-13

Variant appearance in text: rs2071410
PubMed Link: 20707915
Variant Present in the following documents:
  • Main text
  • 1471-2350-11-124.pdf
View BVdb publication page