GRN c.1009C>T ;(p.Q337*)

Variant ID: 17-42428993-C-T

NM_002087.2(GRN):c.1009C>T;(p.Q337*)

This variant was identified in 10 publications

View GRCh38 version.




Publications:


Parkin Levels Decrease in Fibroblasts With Progranulin (PGRN) Pathogenic Variants and in a Cellular Model of PGRN Deficiency.

Frontiers In Molecular Neuroscience
Gaweda-Walerych, Katarzyna K; Walerych, Dawid D; Berdyński, Mariusz M; Buratti, Emanuele E; Zekanowski, Cezary C
Publication Date: 2021

Variant appearance in text: PGRN: Q337X
PubMed Link: 34054428
Variant Present in the following documents:
  • Main text
  • fnmol-14-676478.pdf
  • Data_Sheet_1.pdf
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Frontotemporal lobar degeneration proteinopathies have disparate microscopic patterns of white and grey matter pathology.

Acta Neuropathologica Communications
Giannini, Lucia A A LAA; Peterson, Claire C; Ohm, Daniel D; Xie, Sharon X SX; McMillan, Corey T CT; Raskovsky, Katya K; Massimo, Lauren L; Suh, EunRah E; Van Deerlin, Vivianna M VM; Wolk, David A DA; Trojanowski, John Q JQ; Lee, Edward B EB; Grossman, Murray M; Irwin, David J DJ
Publication Date: 2021-02-23

Variant appearance in text: GRN: 1009C>T; Q337*
PubMed Link: 33622418
Variant Present in the following documents:
  • Main text
  • 40478_2021_Article_1129.pdf
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Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study.

The Lancet. Neurology
Moore, Katrina M KM; Nicholas, Jennifer J; Grossman, Murray M; McMillan, Corey T CT; Irwin, David J DJ; Massimo, Lauren L; Van Deerlin, Vivianna M VM; Warren, Jason D JD; Fox, Nick C NC; Rossor, Martin N MN; Mead, Simon S; Bocchetta, Martina M; Boeve, Bradley F BF; Knopman, David S DS; Graff-Radford, Neill R NR; Forsberg, Leah K LK; Rademakers, Rosa R; Wszolek, Zbigniew K ZK; van Swieten, John C JC; Jiskoot, Lize C LC; Meeter, Lieke H LH; Dopper, Elise Gp EG; Papma, Janne M JM; Snowden, Julie S JS; Saxon, Jennifer J; Jones, Matthew M; Pickering-Brown, Stuart S; Le Ber, Isabelle I; Camuzat, Agnès A; Brice, Alexis A; Caroppo, Paola P; Ghidoni, Roberta R; Pievani, Michela M; Benussi, Luisa L; Binetti, Giuliano G; Dickerson, Bradford C BC; Lucente, Diane D; Krivensky, Samantha S; Graff, Caroline C; Öijerstedt, Linn L; Fallström, Marie M; Thonberg, Håkan H; Ghoshal, Nupur N; Morris, John C JC; Borroni, Barbara B; Benussi, Alberto A; Padovani, Alessandro A; Galimberti, Daniela D; Scarpini, Elio E; Fumagalli, Giorgio G GG; Mackenzie, Ian R IR; Hsiung, Ging-Yuek R GR; Sengdy, Pheth P; Boxer, Adam L AL; Rosen, Howie H; Taylor, Joanne B JB; Synofzik, Matthis M; Wilke, Carlo C; Sulzer, Patricia P; Hodges, John R JR; Halliday, Glenda G; Kwok, John J; Sanchez-Valle, Raquel R; Lladó, Albert A; Borrego-Ecija, Sergi S; Santana, Isabel I; Almeida, Maria Rosário MR; Tábuas-Pereira, Miguel M; Moreno, Fermin F; Barandiaran, Myriam M; Indakoetxea, Begoña B; Levin, Johannes J; Danek, Adrian A; Rowe, James B JB; Cope, Thomas E TE; Otto, Markus M; Anderl-Straub, Sarah S; de Mendonça, Alexandre A; Maruta, Carolina C; Masellis, Mario M; Black, Sandra E SE; Couratier, Philippe P; Lautrette, Geraldine G; Huey, Edward D ED; Sorbi, Sandro S; Nacmias, Benedetta B; Laforce, Robert R; Tremblay, Marie-Pier L ML; Vandenberghe, Rik R; Damme, Philip Van PV; Rogalski, Emily J EJ; Weintraub, Sandra S; Gerhard, Alexander A; Onyike, Chiadi U CU; Ducharme, Simon S; Papageorgiou, Sokratis G SG; Ng, Adeline Su Lyn ASL; Brodtmann, Amy A; Finger, Elizabeth E; Guerreiro, Rita R; Bras, Jose J; Rohrer, Jonathan D JD; ,
Publication Date: 2020-02

Variant appearance in text: GRN: 1009C>T
PubMed Link: 31810826
Variant Present in the following documents:
  • NIHMS1067362-supplement-Supplement.pdf
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Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration.

Archives Of Neurology
Chen-Plotkin, Alice S AS; Martinez-Lage, Maria M; Sleiman, Patrick M A PM; Hu, William W; Greene, Robert R; Wood, Elisabeth McCarty EM; Bing, Shaoxu S; Grossman, Murray M; Schellenberg, Gerard D GD; Hatanpaa, Kimmo J KJ; Weiner, Myron F MF; White, Charles L CL; Brooks, William S WS; Halliday, Glenda M GM; Kril, Jillian J JJ; Gearing, Marla M; Beach, Thomas G TG; Graff-Radford, Neill R NR; Dickson, Dennis W DW; Rademakers, Rosa R; Boeve, Bradley F BF; Pickering-Brown, Stuart M SM; Snowden, Julie J; van Swieten, John C JC; Heutink, Peter P; Seelaar, Harro H; Murrell, Jill R JR; Ghetti, Bernardino B; Spina, Salvatore S; Grafman, Jordan J; Kaye, Jeffrey A JA; Woltjer, Randall L RL; Mesulam, Marsel M; Bigio, Eileen E; Lladó, Albert A; Miller, Bruce L BL; Alzualde, Ainhoa A; Moreno, Fermin F; Rohrer, Jonathan D JD; Mackenzie, Ian R A IR; Feldman, Howard H HH; Hamilton, Ronald L RL; Cruts, Marc M; Engelborghs, Sebastiaan S; De Deyn, Peter P PP; Van Broeckhoven, Christine C; Bird, Thomas D TD; Cairns, Nigel J NJ; Goate, Allison A; Frosch, Matthew P MP; Riederer, Peter F PF; Bogdanovic, Nenad N; Lee, Virginia M Y VM; Trojanowski, John Q JQ; Van Deerlin, Vivianna M VM
Publication Date: 2011-04

Variant appearance in text: GRN: 1009C>T; Q337X
PubMed Link: 21482928
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.

Nature Genetics
Van Deerlin, Vivianna M VM; Sleiman, Patrick M A PM; Martinez-Lage, Maria M; Chen-Plotkin, Alice A; Wang, Li-San LS; Graff-Radford, Neill R NR; Dickson, Dennis W DW; Rademakers, Rosa R; Boeve, Bradley F BF; Grossman, Murray M; Arnold, Steven E SE; Mann, David M A DM; Pickering-Brown, Stuart M SM; Seelaar, Harro H; Heutink, Peter P; van Swieten, John C JC; Murrell, Jill R JR; Ghetti, Bernardino B; Spina, Salvatore S; Grafman, Jordan J; Hodges, John J; Spillantini, Maria Grazia MG; Gilman, Sid S; Lieberman, Andrew P AP; Kaye, Jeffrey A JA; Woltjer, Randall L RL; Bigio, Eileen H EH; Mesulam, Marsel M; Al-Sarraj, Safa S; Troakes, Claire C; Rosenberg, Roger N RN; White, Charles L CL; Ferrer, Isidro I; Lladó, Albert A; Neumann, Manuela M; Kretzschmar, Hans A HA; Hulette, Christine Marie CM; Welsh-Bohmer, Kathleen A KA; Miller, Bruce L BL; Alzualde, Ainhoa A; Lopez de Munain, Adolfo A; McKee, Ann C AC; Gearing, Marla M; Levey, Allan I AI; Lah, James J JJ; Hardy, John J; Rohrer, Jonathan D JD; Lashley, Tammaryn T; Mackenzie, Ian R A IR; Feldman, Howard H HH; Hamilton, Ronald L RL; Dekosky, Steven T ST; van der Zee, Julie J; Kumar-Singh, Samir S; Van Broeckhoven, Christine C; Mayeux, Richard R; Vonsattel, Jean Paul G JP; Troncoso, Juan C JC; Kril, Jillian J JJ; Kwok, John B J JB; Halliday, Glenda M GM; Bird, Thomas D TD; Ince, Paul G PG; Shaw, Pamela J PJ; Cairns, Nigel J NJ; Morris, John C JC; McLean, Catriona Ann CA; DeCarli, Charles C; Ellis, William G WG; Freeman, Stefanie H SH; Frosch, Matthew P MP; Growdon, John H JH; Perl, Daniel P DP; Sano, Mary M; Bennett, David A DA; Schneider, Julie A JA; Beach, Thomas G TG; Reiman, Eric M EM; Woodruff, Bryan K BK; Cummings, Jeffrey J; Vinters, Harry V HV; Miller, Carol A CA; Chui, Helena C HC; Alafuzoff, Irina I; Hartikainen, Päivi P; Seilhean, Danielle D; Galasko, Douglas D; Masliah, Eliezer E; Cotman, Carl W CW; Tuñón, M Teresa MT; Martínez, M Cristina Caballero MC; Munoz, David G DG; Carroll, Steven L SL; Marson, Daniel D; Riederer, Peter F PF; Bogdanovic, Nenad N; Schellenberg, Gerard D GD; Hakonarson, Hakon H; Trojanowski, John Q JQ; Lee, Virginia M-Y VM
Publication Date: 2010-03

Variant appearance in text: GRN: 1009C>T; Q337X
PubMed Link: 20154673
Variant Present in the following documents:
  • NIHMS172758-supplement-1.pdf
View BVdb publication page



The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration.

Archives Of Neurology
Yu, Chang-En CE; Bird, Thomas D TD; Bekris, Lynn M LM; Montine, Thomas J TJ; Leverenz, James B JB; Steinbart, Ellen E; Galloway, Nichole M NM; Feldman, Howard H; Woltjer, Randall R; Miller, Carol A CA; Wood, Elisabeth McCarty EM; Grossman, Murray M; McCluskey, Leo L; Clark, Christopher M CM; Neumann, Manuela M; Danek, Adrian A; Galasko, Douglas R DR; Arnold, Steven E SE; Chen-Plotkin, Alice A; Karydas, Anna A; Miller, Bruce L BL; Trojanowski, John Q JQ; Lee, Virginia M-Y VM; Schellenberg, Gerard D GD; Van Deerlin, Vivianna M VM
Publication Date: 2010-02

Variant appearance in text: GRN: 1009C>T
PubMed Link: 20142524
Variant Present in the following documents:
  • Main text
View BVdb publication page



Brain progranulin expression in GRN-associated frontotemporal lobar degeneration.

Acta Neuropathologica
Chen-Plotkin, Alice S AS; Xiao, Jiping J; Geser, Felix F; Martinez-Lage, Maria M; Grossman, Murray M; Unger, Travis T; Wood, Elisabeth M EM; Van Deerlin, Vivianna M VM; Trojanowski, John Q JQ; Lee, Virginia M-Y VM
Publication Date: 2010-01

Variant appearance in text: GRN: 1009C>T; Q337X
PubMed Link: 19649643
Variant Present in the following documents:
  • Main text
View BVdb publication page



Clinical and pathological continuum of multisystem TDP-43 proteinopathies.

Archives Of Neurology
Geser, Felix F; Martinez-Lage, Maria M; Robinson, John J; Uryu, Kunihiro K; Neumann, Manuela M; Brandmeir, Nicholas J NJ; Xie, Sharon X SX; Kwong, Linda K LK; Elman, Lauren L; McCluskey, Leo L; Clark, Chris M CM; Malunda, Joe J; Miller, Bruce L BL; Zimmerman, Earl A EA; Qian, Jiang J; Van Deerlin, Vivianna V; Grossman, Murray M; Lee, Virginia M-Y VM; Trojanowski, John Q JQ
Publication Date: 2009-02

Variant appearance in text: PGRN: 1009C>T
PubMed Link: 19204154
Variant Present in the following documents:
  • Main text
View BVdb publication page



Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies.

Acta Neuropathologica
Neumann, Manuela M; Kwong, Linda K LK; Lee, Edward B EB; Kremmer, Elisabeth E; Flatley, Andrew A; Xu, Yan Y; Forman, Mark S MS; Troost, Dirk D; Kretzschmar, Hans A HA; Trojanowski, John Q JQ; Lee, Virginia M-Y VM
Publication Date: 2009-02

Variant appearance in text: GRN: Q337X
PubMed Link: 19125255
Variant Present in the following documents:
  • Main text
View BVdb publication page



Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration.

Human Molecular Genetics
Chen-Plotkin, Alice S AS; Geser, Felix F; Plotkin, Joshua B JB; Clark, Chris M CM; Kwong, Linda K LK; Yuan, Wuxing W; Grossman, Murray M; Van Deerlin, Vivianna M VM; Trojanowski, John Q JQ; Lee, Virginia M-Y VM
Publication Date: 2008-05-15

Variant appearance in text: GRN: 1009C>T; Q337X
PubMed Link: 18223198
Variant Present in the following documents:
  • Main text
View BVdb publication page