KCNQ2 c.356A>G ;(p.E119G)

Variant ID: 20-62078131-T-C

NM_172107.2(KCNQ2):c.356A>G;(p.E119G)

This variant was identified in 8 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: KCNQ2: 356A>G; Glu119Gly
PubMed Link: 36823319
Variant Present in the following documents:
  • 41588_2023_1327_MOESM4_ESM.xlsx, sheet 6
View BVdb publication page



Single C-to-T substitution using engineered APOBEC3G-nCas9 base editors with minimum genome- and transcriptome-wide off-target effects.

Science Advances
Lee, Sangsin S; Ding, Ning N; Sun, Yidi Y; Yuan, Tanglong T; Li, Jing J; Yuan, Qichen Q; Liu, Lizhong L; Yang, Jie J; Wang, Qian Q; Kolomeisky, Anatoly B AB; Hilton, Isaac B IB; Zuo, Erwei E; Gao, Xue X
Publication Date: 2020-07

Variant appearance in text: KCNQ2: 356A>G; Glu119Gly
PubMed Link: 32832622
Variant Present in the following documents:
  • aba1773_Data_file_S1.xlsx, sheet 4
  • aba1773_Data_file_S1.xlsx, sheet 2
  • aba1773_Data_file_S1.xlsx, sheet 3
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Identifying mutation hotspots reveals pathogenetic mechanisms of KCNQ2 epileptic encephalopathy.

Scientific Reports
Zhang, Jiaren J; Kim, Eung Chang EC; Chen, Congcong C; Procko, Erik E; Pant, Shashank S; Lam, Kin K; Patel, Jaimin J; Choi, Rebecca R; Hong, Mary M; Joshi, Dhruv D; Bolton, Eric E; Tajkhorshid, Emad E; Chung, Hee Jung HJ
Publication Date: 2020-03-16

Variant appearance in text: Kv7.2: 356A>G
PubMed Link: 32179837
Variant Present in the following documents:
  • 41598_2020_61697_MOESM2_ESM.pdf
View BVdb publication page



Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation.

Genome Research
Traynelis, Joshua J; Silk, Michael M; Wang, Quanli Q; Berkovic, Samuel F SF; Liu, Liping L; Ascher, David B DB; Balding, David J DJ; Petrovski, Slavé S
Publication Date: 2017-10

Variant appearance in text: KCNQ2: 356A>G; Glu119Gly
PubMed Link: 28864458
Variant Present in the following documents:
  • supp_gr.226589.117_Supplemental_Data_S1.xlsx, sheet 1
View BVdb publication page



Ion Channel Genes and Epilepsy: Functional Alteration, Pathogenic Potential, and Mechanism of Epilepsy.

Neuroscience Bulletin
Wei, Feng F; Yan, Li-Min LM; Su, Tao T; He, Na N; Lin, Zhi-Jian ZJ; Wang, Jie J; Shi, Yi-Wu YW; Yi, Yong-Hong YH; Liao, Wei-Ping WP
Publication Date: 2017-08

Variant appearance in text: KCNQ2: E119G
PubMed Link: 28488083
Variant Present in the following documents:
  • Main text
View BVdb publication page



The Voltage-Sensing Domain of K(v)7.2 Channels as a Molecular Target for Epilepsy-Causing Mutations and Anticonvulsants.

Frontiers In Pharmacology
Miceli, Francesco F; Soldovieri, Maria Virginia MV; Iannotti, Fabio Arturo FA; Barrese, Vincenzo V; Ambrosino, Paolo P; Martire, Maria M; Cilio, Maria Roberta MR; Taglialatela, Maurizio M
Publication Date: 2011

Variant appearance in text: Kv7.2: E119G
PubMed Link: 21687499
Variant Present in the following documents:
  • fphar-02-00002.pdf
View BVdb publication page



Nervous system KV7 disorders: breakdown of a subthreshold brake.

The Journal Of Physiology
Maljevic, Snezana S; Wuttke, Thomas V TV; Lerche, Holger H
Publication Date: 2008-04-01

Variant appearance in text: KCNQ2: E119G
PubMed Link: 18238816
Variant Present in the following documents:
  • Main text
View BVdb publication page



Neutralization of a negative charge in the S1-S2 region of the KV7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsy.

The Journal Of Physiology
Wuttke, Thomas V TV; Penzien, Johann J; Fauler, Michael M; Seebohm, Guiscard G; Lehmann-Horn, Frank F; Lerche, Holger H; Jurkat-Rott, Karin K
Publication Date: 2008-01-15

Variant appearance in text: KCNQ2: E119G
PubMed Link: 18006581
Variant Present in the following documents:
  • Main text
View BVdb publication page