CD6 c.50-13434C>G

Variant ID: 11-60760612-C-G

NM_006725.4(CD6):c.50-13434C>G

This variant was identified in 31 publications

View GRCh38 version.




Publications:


Analysis of herpesvirus infection and genome single nucleotide polymorphism risk factors in multiple sclerosis, Volga federal district, Russia.

Frontiers In Immunology
Lezhnyova, Vera V; Davidyuk, Yuriy Y; Mullakhmetova, Asia A; Markelova, Maria M; Zakharov, Alexander A; Khaiboullina, Svetlana S; Martynova, Ekaterina E
Publication Date: 2022

Variant appearance in text: rs17824933
PubMed Link: 36451826
Variant Present in the following documents:
  • Main text
  • fimmu-13-1010605.pdf
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The dual role of CD6 as a therapeutic target in cancer and autoimmune disease.

Frontiers In Medicine
Gurrea-Rubio, Mikel M; Fox, David A DA
Publication Date: 2022

Variant appearance in text: rs17824933
PubMed Link: 36275816
Variant Present in the following documents:
  • Main text
  • fmed-09-1026521.pdf
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Gene variation impact on prostate cancer progression: Lymphocyte modulator, activation, and cell adhesion gene variant contribution.

The Prostate
Casadó-Llombart, Sergi S; Ajami, Tarek T; Consuegra-Fernández, Marta M; Carreras, Esther E; Aranda, Fernando F; Armiger, Noelia N; Alcaraz, Antonio A; Mengual, Lourdes L; Lozano, Francisco F
Publication Date: 2022-10

Variant appearance in text: rs17824933
PubMed Link: 35767366
Variant Present in the following documents:
  • Main text
  • PROS-82-1331.pdf
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Gene Variation at Immunomodulatory and Cell Adhesion Molecules Loci Impacts Primary Sjögren's Syndrome.

Frontiers In Medicine
Casadó-Llombart, Sergi S; Gheitasi, Hoda H; Ariño, Silvia S; Consuegra-Fernández, Marta M; Armiger-Borràs, Noelia N; Kostov, Belchin B; Ramos-Casals, Manuel M; Brito-Zerón, Pilar P; Lozano, Francisco F
Publication Date: 2022

Variant appearance in text: rs17824933
PubMed Link: 35372412
Variant Present in the following documents:
  • Main text
  • fmed-09-822290.pdf
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Contribution of Evolutionary Selected Immune Gene Polymorphism to Immune-Related Disorders: The Case of Lymphocyte Scavenger Receptors CD5 and CD6.

International Journal Of Molecular Sciences
Casadó-Llombart, Sergi S; Velasco-de Andrés, María M; Català, Cristina C; Leyton-Pereira, Alejandra A; Lozano, Francisco F; Bosch, Elena E
Publication Date: 2021-05-18

Variant appearance in text: rs17824933
PubMed Link: 34070159
Variant Present in the following documents:
  • Main text
  • ijms-22-05315.pdf
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Replication analysis of variants associated with multiple sclerosis risk.

Scientific Reports
Dashti, Mohammad M; Ateyah, Khadijah K; Alroughani, Raed R; Al-Temaimi, Rabeah R
Publication Date: 2020-04-30

Variant appearance in text: rs17824933
PubMed Link: 32355262
Variant Present in the following documents:
  • 41598_2020_64432_MOESM1_ESM.pdf
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Breakdown of multiple sclerosis genetics to identify an integrated disease network and potential variant mechanisms.

Physiological Genomics
Shepard, C Joy CJ; Cline, Sara G SG; Hinds, David D; Jahanbakhsh, Seyedehameneh S; Prokop, Jeremy W JW
Publication Date: 2019-11-01

Variant appearance in text: rs17824933
PubMed Link: 31482761
Variant Present in the following documents:
  • Main text
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Multiple Sclerosis in India.

Annals Of Indian Academy Of Neurology
Goyal, Vinay V
Publication Date: 2018

Variant appearance in text: rs17824933
PubMed Link: 30122832
Variant Present in the following documents:
  • AIAN-21-95.pdf
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Failure of a T cell regulator: CD6 contributes to the aggravation of autoimmune inflammation.

Cellular & Molecular Immunology
Meyer, Anja A; Kofler, David M DM
Publication Date: 2019-09

Variant appearance in text: rs17824933
PubMed Link: 30002450
Variant Present in the following documents:
  • Main text
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Genetic and experimental evidence for the involvement of the CD6 lymphocyte receptor in psoriasis.

Cellular & Molecular Immunology
Consuegra-Fernández, Marta M; Julià, Marc M; Martínez-Florensa, Mario M; Aranda, Fernando F; Català, Cristina C; Armiger-Borràs, Noelia N; Arias, María-Teresa MT; Santiago, Francisca F; Guilabert, Antonio A; Esteve, Anna A; Muñoz, Carlos C; Ferrándiz, Carlos C; Carrascosa, José-Manuel JM; Pedrosa, Edurne E; Romaní, Jorge J; Alsina, Mercè M; Mascaró-Galy, José-Manuel JM; Lozano, Francisco F
Publication Date: 2018-10

Variant appearance in text: rs17824933
PubMed Link: 29225340
Variant Present in the following documents:
  • Main text
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Genetic variations in the Dravidian population of South West coast of India: Implications in designing case-control studies.

The Indian Journal Of Medical Research
D'Cunha, Anitha A; Pandit, Lekha L; Malli, Chaithra C
Publication Date: 2017-06

Variant appearance in text: rs17824933
PubMed Link: 29067977
Variant Present in the following documents:
  • IJMR-145-753.pdf
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ALCAM (CD166) is involved in extravasation of monocytes rather than T cells across the blood-brain barrier.

Journal Of Cerebral Blood Flow And Metabolism : Official Journal Of The International Society Of Cerebral Blood Flow And Metabolism
Lyck, Ruth R; Lécuyer, Marc-André MA; Abadier, Michael M; Wyss, Christof B CB; Matti, Christoph C; Rosito, Maria M; Enzmann, Gaby G; Zeis, Thomas T; Michel, Laure L; García Martín, Ana B AB; Sallusto, Federica F; Gosselet, Fabien F; Deutsch, Urban U; Weiner, Joshua A JA; Schaeren-Wiemers, Nicole N; Prat, Alexandre A; Engelhardt, Britta B
Publication Date: 2017-08

Variant appearance in text: rs17824933
PubMed Link: 28273717
Variant Present in the following documents:
  • Main text
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CD6 gene polymorphism rs17824933 is associated with multiple sclerosis in Indian population.

Annals Of Indian Academy Of Neurology
D'Cunha, Mary Anitha MA; Pandit, Lekha L; Malli, Chaithra C
Publication Date: 2016

Variant appearance in text: rs17824933
PubMed Link: 27994359
Variant Present in the following documents:
  • Main text
  • AIAN-19-491.pdf
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Genetic polymorphisms of cell adhesion molecules in Behcet's disease in a Chinese Han population.

Scientific Reports
Zheng, Minming M; Zhang, Lijun L; Yu, Hongsong H; Hu, Jiayue J; Cao, Qingfeng Q; Huang, Guo G; Huang, Yang Y; Yuan, Gangxiang G; Kijlstra, Aize A; Yang, Peizeng P
Publication Date: 2016-04-25

Variant appearance in text: rs17824933
PubMed Link: 27108704
Variant Present in the following documents:
  • Main text
  • srep24974.pdf
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Genetic basis of autoimmunity.

The Journal Of Clinical Investigation
Marson, Alexander A; Housley, William J WJ; Hafler, David A DA
Publication Date: 2015-06

Variant appearance in text: rs17824933
PubMed Link: 26030227
Variant Present in the following documents:
  • Main text
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Multiple sclerosis susceptibility genes: associations with relapse severity and recovery.

Plos One
Mowry, Ellen M EM; Carey, Robert F RF; Blasco, Maria R MR; Pelletier, Jean J; Duquette, Pierre P; Villoslada, Pablo P; Malikova, Irina I; Roger, Elaine E; Kinkel, R Phillip RP; McDonald, Jamie J; Bacchetti, Peter P; Waubant, Emmanuelle E
Publication Date: 2013

Variant appearance in text: rs17824933
PubMed Link: 24130709
Variant Present in the following documents:
  • Main text
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Progress in multiple sclerosis genetics.

Current Genomics
Goris, An A; Pauwels, Ine I; Dubois, Bénédicte B
Publication Date: 2012-12

Variant appearance in text: rs17824933
PubMed Link: 23730204
Variant Present in the following documents:
  • Main text
  • CG-13-646.pdf
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Fine mapping and functional analysis of the multiple sclerosis risk gene CD6.

Plos One
Swaminathan, Bhairavi B; Cuapio, Angélica A; Alloza, Iraide I; Matesanz, Fuencisla F; Alcina, Antonio A; García-Barcina, Maria M; Fedetz, Maria M; Fernández, Oscar O; Lucas, Miguel M; Orpez, Teresa T; Pinto-Medel, M Jesus MJ; Otaegui, David D; Olascoaga, Javier J; Urcelay, Elena E; Ortiz, Miguel A MA; Arroyo, Rafael R; Oksenberg, Jorge R JR; Antigüedad, Alfredo A; Tolosa, Eva E; Vandenbroeck, Koen K
Publication Date: 2013

Variant appearance in text: rs17824933
PubMed Link: 23638056
Variant Present in the following documents:
  • Main text
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RNA-Seq and human complex diseases: recent accomplishments and future perspectives.

European Journal Of Human Genetics : Ejhg
Costa, Valerio V; Aprile, Marianna M; Esposito, Roberta R; Ciccodicola, Alfredo A
Publication Date: 2013-02

Variant appearance in text: rs17824933
PubMed Link: 22739340
Variant Present in the following documents:
  • Main text
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The genetics of multiple sclerosis: an up-to-date review.

Immunological Reviews
Gourraud, Pierre-Antoine PA; Harbo, Hanne F HF; Hauser, Stephen L SL; Baranzini, Sergio E SE
Publication Date: 2012-07

Variant appearance in text: rs17824933
PubMed Link: 22725956
Variant Present in the following documents:
  • Main text
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Rationale for Targeting CD6 as a Treatment for Autoimmune Diseases.

Arthritis
Alonso-Ramirez, Ruby R; Loisel, Séverine S; Buors, Caroline C; Pers, Jacques-Olivier JO; Montero, Enrique E; Youinou, Pierre P; Renaudineau, Yves Y
Publication Date: 2010

Variant appearance in text: rs17824933
PubMed Link: 22076177
Variant Present in the following documents:
  • Main text
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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: rs17824933
PubMed Link: 21833088
Variant Present in the following documents:
  • NIHMS36028-supplement-1.pdf
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The genetic association of variants in CD6, TNFRSF1A and IRF8 to multiple sclerosis: a multicenter case-control study.

Plos One
,
Publication Date: 2011-04-28

Variant appearance in text: rs17824933
PubMed Link: 21552549
Variant Present in the following documents:
  • Main text
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Aggregation of multiple sclerosis genetic risk variants in multiple and single case families.

Annals Of Neurology
Gourraud, Pierre-Antoine PA; McElroy, Joseph P JP; Caillier, Stacy J SJ; Johnson, Britt A BA; Santaniello, Adam A; Hauser, Stephen L SL; Oksenberg, Jorge R JR
Publication Date: 2011-01

Variant appearance in text: rs17824933
PubMed Link: 21280076
Variant Present in the following documents:
  • Main text
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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: rs17824933
PubMed Link: 21247752
Variant Present in the following documents:
  • Main text
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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: rs17824933
PubMed Link: 20405052
Variant Present in the following documents:
  • Main text
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Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come.

American Journal Of Human Genetics
, ; Bush, William S WS; Sawcer, Stephen J SJ; de Jager, Philip L PL; Oksenberg, Jorge R JR; McCauley, Jacob L JL; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL
Publication Date: 2010-04-09

Variant appearance in text: rs17824933
PubMed Link: 20362272
Variant Present in the following documents:
  • Main text
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What role for genetics in the prediction of multiple sclerosis?

Annals Of Neurology
Sawcer, Stephen S; Ban, Maria M; Wason, James J; Dudbridge, Frank F
Publication Date: 2010-01

Variant appearance in text: rs17824933
PubMed Link: 20186855
Variant Present in the following documents:
  • Main text
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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: rs17824933
PubMed Link: 19865102
Variant Present in the following documents:
  • Main text
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Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing.

Human Molecular Genetics
Heap, Graham A GA; Yang, Jennie H M JH; Downes, Kate K; Healy, Barry C BC; Hunt, Karen A KA; Bockett, Nicholas N; Franke, Lude L; Dubois, Patrick C PC; Mein, Charles A CA; Dobson, Richard J RJ; Albert, Thomas J TJ; Rodesch, Matthew J MJ; Clayton, David G DG; Todd, John A JA; van Heel, David A DA; Plagnol, Vincent V
Publication Date: 2010-01-01

Variant appearance in text: rs17824933
PubMed Link: 19825846
Variant Present in the following documents:
  • Main text
  • ddp473.pdf
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Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.

Nature Genetics
De Jager, Philip L PL; Jia, Xiaoming X; Wang, Joanne J; de Bakker, Paul I W PI; Ottoboni, Linda L; Aggarwal, Neelum T NT; Piccio, Laura L; Raychaudhuri, Soumya S; Tran, Dong D; Aubin, Cristin C; Briskin, Rebeccah R; Romano, Susan S; , ; Baranzini, Sergio E SE; McCauley, Jacob L JL; Pericak-Vance, Margaret A MA; Haines, Jonathan L JL; Gibson, Rachel A RA; Naeglin, Yvonne Y; Uitdehaag, Bernard B; Matthews, Paul M PM; Kappos, Ludwig L; Polman, Chris C; McArdle, Wendy L WL; Strachan, David P DP; Evans, Denis D; Cross, Anne H AH; Daly, Mark J MJ; Compston, Alastair A; Sawcer, Stephen J SJ; Weiner, Howard L HL; Hauser, Stephen L SL; Hafler, David A DA; Oksenberg, Jorge R JR
Publication Date: 2009-07

Variant appearance in text: rs17824933
PubMed Link: 19525953
Variant Present in the following documents:
  • Main text
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