GPC5 c.1562-186649G>A

Variant ID: 13-93331886-G-A

NM_004466.4(GPC5):c.1562-186649G>A

This variant was identified in 11 publications

View GRCh38 version.




Publications:


A Comprehensive Review on the Role of Genetic Factors in Neuromyelitis Optica Spectrum Disorder.

Frontiers In Immunology
Ghafouri-Fard, Soudeh S; Azimi, Tahereh T; Taheri, Mohammad M
Publication Date: 2021

Variant appearance in text: rs9523762
PubMed Link: 34675927
Variant Present in the following documents:
  • Main text
  • fimmu-12-737673.pdf
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An investigation of genetic polymorphisms in heparan sulfate proteoglycan core proteins and key modification enzymes in an Australian Caucasian multiple sclerosis population.

Human Genomics
Okolicsanyi, Rachel K RK; Bluhm, Julia J; Miller, Cassandra C; Griffiths, Lyn R LR; Haupt, Larisa M LM
Publication Date: 2020-05-12

Variant appearance in text: rs9523762
PubMed Link: 32398079
Variant Present in the following documents:
  • Main text
  • 40246_2020_Article_264.pdf
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Exon-focused genome-wide association study of obsessive-compulsive disorder and shared polygenic risk with schizophrenia.

Translational Psychiatry
Costas, J J; Carrera, N N; Alonso, P P; Gurriarán, X X; Segalàs, C C; Real, E E; López-Solà, C C; Mas, S S; Gassó, P P; Domènech, L L; Morell, M M; Quintela, I I; Lázaro, L L; Menchón, J M JM; Estivill, X X; Carracedo, Á Á
Publication Date: 2016-03-29

Variant appearance in text: rs9523762
PubMed Link: 27023174
Variant Present in the following documents:
  • Main text
  • tp201634a.pdf
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Re-annotation of presumed noncoding disease/trait-associated genetic variants by integrative analyses.

Scientific Reports
Chen, Geng G; Yu, Dianke D; Chen, Jiwei J; Cao, Ruifang R; Yang, Juan J; Wang, Huan H; Ji, Xiangjun X; Ning, Baitang B; Shi, Tieliu T
Publication Date: 2015-03-30

Variant appearance in text: rs9523762
PubMed Link: 25819875
Variant Present in the following documents:
  • srep09453-s1.pdf
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A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1).

Plos Genetics
Rubicz, Rohina R; Yolken, Robert R; Drigalenko, Eugene E; Carless, Melanie A MA; Dyer, Thomas D TD; Bauman, Lara L; Melton, Phillip E PE; Kent, Jack W JW; Harley, John B JB; Curran, Joanne E JE; Johnson, Matthew P MP; Cole, Shelley A SA; Almasy, Laura L; Moses, Eric K EK; Dhurandhar, Nikhil V NV; Kraig, Ellen E; Blangero, John J; Leach, Charles T CT; Göring, Harald H H HH
Publication Date: 2013

Variant appearance in text: rs9523762
PubMed Link: 23326239
Variant Present in the following documents:
  • Main text
  • pgen.1003147.pdf
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Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.

Nature
, ; , ; Sawcer, Stephen S; Hellenthal, Garrett G; Pirinen, Matti M; Spencer, Chris C A CC; Patsopoulos, Nikolaos A NA; Moutsianas, Loukas L; Dilthey, Alexander A; Su, Zhan Z; Freeman, Colin C; Hunt, Sarah E SE; Edkins, Sarah S; Gray, Emma E; Booth, David R DR; Potter, Simon C SC; Goris, An A; Band, Gavin G; Oturai, Annette Bang AB; Strange, Amy A; Saarela, Janna J; Bellenguez, Céline C; Fontaine, Bertrand B; Gillman, Matthew M; Hemmer, Bernhard B; Gwilliam, Rhian R; Zipp, Frauke F; Jayakumar, Alagurevathi A; Martin, Roland R; Leslie, Stephen S; Hawkins, Stanley S; Giannoulatou, Eleni E; D'alfonso, Sandra S; Blackburn, Hannah H; Martinelli Boneschi, Filippo F; Liddle, Jennifer J; Harbo, Hanne F HF; Perez, Marc L ML; Spurkland, Anne A; Waller, Matthew J MJ; Mycko, Marcin P MP; Ricketts, Michelle M; Comabella, Manuel M; Hammond, Naomi N; Kockum, Ingrid I; McCann, Owen T OT; Ban, Maria M; Whittaker, Pamela P; Kemppinen, Anu A; Weston, Paul P; Hawkins, Clive C; Widaa, Sara S; Zajicek, John J; Dronov, Serge S; Robertson, Neil N; Bumpstead, Suzannah J SJ; Barcellos, Lisa F LF; Ravindrarajah, Rathi R; Abraham, Roby R; Alfredsson, Lars L; Ardlie, Kristin K; Aubin, Cristin C; Baker, Amie A; Baker, Katharine K; Baranzini, Sergio E SE; Bergamaschi, Laura L; Bergamaschi, Roberto R; Bernstein, Allan A; Berthele, Achim A; Boggild, Mike M; Bradfield, Jonathan P JP; Brassat, David D; Broadley, Simon A SA; Buck, Dorothea D; Butzkueven, Helmut H; Capra, Ruggero R; Carroll, William M WM; Cavalla, Paola P; Celius, Elisabeth G EG; Cepok, Sabine S; Chiavacci, Rosetta R; Clerget-Darpoux, Françoise F; Clysters, Katleen K; Comi, Giancarlo G; Cossburn, Mark M; Cournu-Rebeix, Isabelle I; Cox, Mathew B MB; Cozen, Wendy W; Cree, Bruce A C BA; Cross, Anne H AH; Cusi, Daniele D; Daly, Mark J MJ; Davis, Emma E; de Bakker, Paul I W PI; Debouverie, Marc M; D'hooghe, Marie Beatrice MB; Dixon, Katherine K; Dobosi, Rita R; Dubois, Bénédicte B; Ellinghaus, David D; Elovaara, Irina I; Esposito, Federica F; Fontenille, Claire C; Foote, Simon S; Franke, Andre A; Galimberti, Daniela D; Ghezzi, Angelo A; Glessner, Joseph J; Gomez, Refujia R; Gout, Olivier O; Graham, Colin C; Grant, Struan F A SF; Guerini, Franca Rosa FR; Hakonarson, Hakon H; Hall, Per P; Hamsten, Anders A; Hartung, Hans-Peter HP; Heard, Rob N RN; Heath, Simon S; Hobart, Jeremy J; Hoshi, Muna M; Infante-Duarte, Carmen C; Ingram, Gillian G; Ingram, Wendy W; Islam, Talat T; Jagodic, Maja M; Kabesch, Michael M; Kermode, Allan G AG; Kilpatrick, Trevor J TJ; Kim, Cecilia C; Klopp, Norman N; Koivisto, Keijo K; Larsson, Malin M; Lathrop, Mark M; Lechner-Scott, Jeannette S JS; Leone, Maurizio A MA; Leppä, Virpi V; Liljedahl, Ulrika U; Bomfim, Izaura Lima IL; Lincoln, Robin R RR; Link, Jenny J; Liu, Jianjun J; Lorentzen, Aslaug R AR; Lupoli, Sara S; Macciardi, Fabio F; Mack, Thomas T; Marriott, Mark M; Martinelli, Vittorio V; Mason, Deborah D; McCauley, Jacob L JL; Mentch, Frank F; Mero, Inger-Lise IL; Mihalova, Tania T; Montalban, Xavier X; Mottershead, John J; Myhr, Kjell-Morten KM; Naldi, Paola P; Ollier, William W; Page, Alison A; Palotie, Aarno A; Pelletier, Jean J; Piccio, Laura L; Pickersgill, Trevor T; Piehl, Fredrik F; Pobywajlo, Susan S; Quach, Hong L HL; Ramsay, Patricia P PP; Reunanen, Mauri M; Reynolds, Richard R; Rioux, John D JD; Rodegher, Mariaemma M; Roesner, Sabine S; Rubio, Justin P JP; Rückert, Ina-Maria IM; Salvetti, Marco M; Salvi, Erika E; Santaniello, Adam A; Schaefer, Catherine A CA; Schreiber, Stefan S; Schulze, Christian C; Scott, Rodney J RJ; Sellebjerg, Finn F; Selmaj, Krzysztof W KW; Sexton, David D; Shen, Ling L; Simms-Acuna, Brigid B; Skidmore, Sheila S; Sleiman, Patrick M A PM; Smestad, Cathrine C; Sørensen, Per Soelberg PS; Søndergaard, Helle Bach HB; Stankovich, Jim J; Strange, Richard C RC; Sulonen, Anna-Maija AM; Sundqvist, Emilie E; Syvänen, Ann-Christine AC; Taddeo, Francesca F; Taylor, Bruce B; Blackwell, Jenefer M JM; Tienari, Pentti P; Bramon, Elvira E; Tourbah, Ayman A; Brown, Matthew A MA; Tronczynska, Ewa E; Casas, Juan P JP; Tubridy, Niall N; Corvin, Aiden A; Vickery, Jane J; Jankowski, Janusz J; Villoslada, Pablo P; Markus, Hugh S HS; Wang, Kai K; Mathew, Christopher G CG; Wason, James J; Palmer, Colin N A CN; Wichmann, H-Erich HE; Plomin, Robert R; Willoughby, Ernest E; Rautanen, Anna A; Winkelmann, Juliane J; Wittig, Michael M; Trembath, Richard C RC; Yaouanq, Jacqueline J; Viswanathan, Ananth C AC; Zhang, Haitao H; Wood, Nicholas W NW; Zuvich, Rebecca R; Deloukas, Panos P; Langford, Cordelia C; Duncanson, Audrey A; Oksenberg, Jorge R JR; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL; Olsson, Tomas T; Hillert, Jan J; Ivinson, Adrian J AJ; De Jager, Philip L PL; Peltonen, Leena L; Stewart, Graeme J GJ; Hafler, David A DA; Hauser, Stephen L SL; McVean, Gil G; Donnelly, Peter P; Compston, Alastair A
Publication Date: 2011-08-10

Variant appearance in text: rs9523762
PubMed Link: 21833088
Variant Present in the following documents:
  • NIHMS36028-supplement-1.pdf
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Revealing the genetic basis of multiple sclerosis: are we there yet?

Current Opinion In Genetics & Development
Baranzini, Sergio E SE
Publication Date: 2011-06

Variant appearance in text: rs9523762
PubMed Link: 21247752
Variant Present in the following documents:
  • Main text
View BVdb publication page



The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.

Plos One
Handel, Adam E AE; Handunnetthi, Lahiru L; Berlanga, Antonio J AJ; Watson, Corey T CT; Morahan, Julia M JM; Ramagopalan, Sreeram V SV
Publication Date: 2010-04-13

Variant appearance in text: rs9523762
PubMed Link: 20405052
Variant Present in the following documents:
  • Main text
View BVdb publication page



The genetic aspects of multiple sclerosis.

Annals Of Indian Academy Of Neurology
Sawcer, Stephen S
Publication Date: 2009-10

Variant appearance in text: rs9523762
PubMed Link: 20182566
Variant Present in the following documents:
  • Main text
View BVdb publication page



Multiple sclerosis susceptibility alleles in African Americans.

Genes And Immunity
Johnson, B A BA; Wang, J J; Taylor, E M EM; Caillier, S J SJ; Herbert, J J; Khan, O A OA; Cross, A H AH; De Jager, P L PL; Gourraud, P-A F PA; Cree, B C A BC; Hauser, S L SL; Oksenberg, J R JR
Publication Date: 2010-06

Variant appearance in text: rs9523762
PubMed Link: 19865102
Variant Present in the following documents:
  • Main text
  • nihms146120.pdf
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Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.

Human Molecular Genetics
Baranzini, Sergio E SE; Wang, Joanne J; Gibson, Rachel A RA; Galwey, Nicholas N; Naegelin, Yvonne Y; Barkhof, Frederik F; Radue, Ernst-Wilhelm EW; Lindberg, Raija L P RL; Uitdehaag, Bernard M G BM; Johnson, Michael R MR; Angelakopoulou, Aspasia A; Hall, Leslie L; Richardson, Jill C JC; Prinjha, Rab K RK; Gass, Achim A; Geurts, Jeroen J G JJ; Kragt, Jolijn J; Sombekke, Madeleine M; Vrenken, Hugo H; Qualley, Pamela P; Lincoln, Robin R RR; Gomez, Refujia R; Caillier, Stacy J SJ; George, Michaela F MF; Mousavi, Hourieh H; Guerrero, Rosa R; Okuda, Darin T DT; Cree, Bruce A C BA; Green, Ari J AJ; Waubant, Emmanuelle E; Goodin, Douglas S DS; Pelletier, Daniel D; Matthews, Paul M PM; Hauser, Stephen L SL; Kappos, Ludwig L; Polman, Chris H CH; Oksenberg, Jorge R JR
Publication Date: 2009-02-15

Variant appearance in text: rs9523762
PubMed Link: 19010793
Variant Present in the following documents:
  • Main text
View BVdb publication page