NTN1 c.1018+5411A>G

Variant ID: 17-8932119-A-G

NM_004822.2(NTN1):c.1018+5411A>G

This variant was identified in 13 publications

View GRCh38 version.




Publications:


Exploring the Molecular Mechanism of lncRNA-miRNA-mRNA Networks in Non-Syndromic Cleft Lip with or without Cleft Palate.

International Journal Of General Medicine
Wang, Xiangpu X; Guo, Siyuan S; Zhou, Xinli X; Wang, Yupei Y; Zhang, Ting T; Chen, Renji R
Publication Date: 2021

Variant appearance in text: rs4791774
PubMed Link: 34938111
Variant Present in the following documents:
  • Main text
  • ijgm-14-9931.pdf
View BVdb publication page



Editing GWAS: experimental approaches to dissect and exploit disease-associated genetic variation.

Genome Medicine
Rao, Shuquan S; Yao, Yao Y; Bauer, Daniel E DE
Publication Date: 2021-03-10

Variant appearance in text: rs4791774
PubMed Link: 33691767
Variant Present in the following documents:
  • Main text
  • 13073_2021_Article_857.pdf
View BVdb publication page



Association analysis of GWAS hits and non-syndromic cleft lip with/without palate with cleft alveolar in Han population of western China.

International Journal Of Clinical And Experimental Pathology
Duan, Shijun S; Shi, Jiayu J; Shi, Bing B; Jia, Zhonglin Z
Publication Date: 2020

Variant appearance in text: rs4791774
PubMed Link: 33165418
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gene-gene interactions between BMP4 and ARHGAP29 among non-syndromic cleft lip only (NSCLO) trios from western Han Chinese population.

International Journal Of Clinical And Experimental Pathology
Wang, Yiru Y; Shi, Jiayu J; Zheng, Qian Q; Shi, Bing B; Jia, Zhonglin Z
Publication Date: 2020

Variant appearance in text: rs4791774
PubMed Link: 32211112
Variant Present in the following documents:
  • Main text
View BVdb publication page



The functional variant of NTN1 contributes to the risk of nonsyndromic cleft lip with or without cleft palate.

European Journal Of Human Genetics : Ejhg
Li, Dandan D; Zhu, Guirong G; Lou, Shu S; Ma, Lan L; Zhang, Chi C; Pan, Yongchu Y; Wang, Lin L
Publication Date: 2020-04

Variant appearance in text: rs4791774
PubMed Link: 31780810
Variant Present in the following documents:
  • Main text
  • 41431_2019_Article_549.pdf
View BVdb publication page



Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft.

Plos Genetics
Huang, Lulin L; Jia, Zhonglin Z; Shi, Yi Y; Du, Qin Q; Shi, Jiayu J; Wang, Ziyan Z; Mou, Yandong Y; Wang, Qingwei Q; Zhang, Bihe B; Wang, Qing Q; Ma, Shi S; Lin, He H; Duan, Shijun S; Yin, Bin B; Lin, Yansong Y; Wang, Yiru Y; Jiang, Dan D; Hao, Fang F; Zhang, Lin L; Wang, Haixin H; Jiang, Suyuan S; Xu, Huijuan H; Yang, Chengwei C; Li, Chenghao C; Li, Jingtao J; Shi, Bing B; Yang, Zhenglin Z
Publication Date: 2019-10

Variant appearance in text: rs4791774
PubMed Link: 31609978
Variant Present in the following documents:
  • Main text
  • pgen.1008357.pdf
View BVdb publication page



Machine Learning Models for Genetic Risk Assessment of Infants with Non-syndromic Orofacial Cleft.

Genomics, Proteomics & Bioinformatics
Zhang, Shi-Jian SJ; Meng, Peiqi P; Zhang, Jieni J; Jia, Peizeng P; Lin, Jiuxiang J; Wang, Xiangfeng X; Chen, Feng F; Wei, Xiaoxing X
Publication Date: 2018-10

Variant appearance in text: rs4791774
PubMed Link: 30578914
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genomic analyses in African populations identify novel risk loci for cleft palate.

Human Molecular Genetics
Butali, Azeez A; Mossey, Peter A PA; Adeyemo, Wasiu L WL; Eshete, Mekonen A MA; Gowans, Lord J J LJJ; Busch, Tamara D TD; Jain, Deepti D; Yu, Wenjie W; Huan, Liu L; Laurie, Cecelia A CA; Laurie, Cathy C CC; Nelson, Sarah S; Li, Mary M; Sanchez-Lara, Pedro A PA; Magee, William P WP; Magee, Kathleen S KS; Auslander, Allyn A; Brindopke, Frederick F; Kay, Denise M DM; Caggana, Michele M; Romitti, Paul A PA; Mills, James L JL; Audu, Rosemary R; Onwuamah, Chika C; Oseni, Ganiyu O GO; Owais, Arwa A; James, Olutayo O; Olaitan, Peter B PB; Aregbesola, Babatunde S BS; Braimah, Ramat O RO; Oginni, Fadekemi O FO; Oladele, Ayodeji O AO; Bello, Saidu A SA; Rhodes, Jennifer J; Shiang, Rita R; Donkor, Peter P; Obiri-Yeboah, Solomon S; Arthur, Fareed Kow Nanse FKN; Twumasi, Peter P; Agbenorku, Pius P; Plange-Rhule, Gyikua G; Oti, Alexander Acheampong AA; Ogunlewe, Olugbenga M OM; Oladega, Afisu A AA; Adekunle, Adegbayi A AA; Erinoso, Akinwunmi O AO; Adamson, Olatunbosun O OO; Elufowoju, Abosede A AA; Ayelomi, Oluwanifemi I OI; Hailu, Taiye T; Hailu, Abiye A; Demissie, Yohannes Y; Derebew, Miliard M; Eliason, Steve S; Romero-Bustillous, Miguel M; Lo, Cynthia C; Park, James J; Desai, Shaan S; Mohammed, Muiawa M; Abate, Firke F; Abdur-Rahman, Lukman O LO; Anand, Deepti D; Saadi, Irfaan I; Oladugba, Abimibola V AV; Lachke, Salil A SA; Amendt, Brad A BA; Rotimi, Charles N CN; Marazita, Mary L ML; Cornell, Robert A RA; Murray, Jeffrey C JC; Adeyemo, Adebowale A AA
Publication Date: 2019-03-15

Variant appearance in text: rs4791774
PubMed Link: 30452639
Variant Present in the following documents:
  • Main text
View BVdb publication page



Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation.

Frontiers In Genetics
Indencleef, Karlijne K; Roosenboom, Jasmien J; Hoskens, Hanne H; White, Julie D JD; Shriver, Mark D MD; Richmond, Stephen S; Peeters, Hilde H; Feingold, Eleanor E; Marazita, Mary L ML; Shaffer, John R JR; Weinberg, Seth M SM; Hens, Greet G; Claes, Peter P
Publication Date: 2018

Variant appearance in text: rs4791774
PubMed Link: 30410503
Variant Present in the following documents:
  • Main text
  • fgene-09-00502.pdf
View BVdb publication page



Item-level analyses reveal genetic heterogeneity in neuroticism.

Nature Communications
Nagel, Mats M; Watanabe, Kyoko K; Stringer, Sven S; Posthuma, Danielle D; van der Sluis, Sophie S
Publication Date: 2018-03-02

Variant appearance in text: rs4791774
PubMed Link: 29500382
Variant Present in the following documents:
  • 41467_2018_3242_MOESM2_ESM.pdf
View BVdb publication page



Association between PAX7 and NTN1 gene polymorphisms and nonsyndromic orofacial clefts in a northern Chinese population.

Medicine
Guo, Qiang Q; Li, Dongmei D; Meng, Xiangbiao X; Liu, Tingting T; Shi, Jinna J; Hao, Yanru Y; Jiao, Xiaohui X; Lv, Kewen K; Hu, Tenglong T; Song, Tao T
Publication Date: 2017-05

Variant appearance in text: rs4791774
PubMed Link: 28489749
Variant Present in the following documents:
  • Main text
  • medi-96-e6724.pdf
View BVdb publication page



Genetic polymorphism of nonsyndromic cleft lip with or without cleft palate is associated with developmental dyslexia in Chinese school-aged populations.

Journal Of Human Genetics
Wang, Bin B; Zhou, Yuxi Y; Leng, Song S; Zheng, Liyuan L; Lv, Hong H; Wang, Fei F; Tan, Li-Hai LH; Sun, Yimin Y
Publication Date: 2017-02

Variant appearance in text: rs4791774
PubMed Link: 27734840
Variant Present in the following documents:
  • Main text
View BVdb publication page



A comprehensive genetic study on left atrium size in Caribbean Hispanics identifies potential candidate genes in 17p10.

Circulation. Cardiovascular Genetics
Wang, Liyong L; Di Tullio, Marco R MR; Beecham, Ashley A; Slifer, Susan S; Rundek, Tatjana T; Homma, Shunichi S; Blanton, Susan H SH; Sacco, Ralph L RL
Publication Date: 2010-08

Variant appearance in text: rs4791774
PubMed Link: 20562446
Variant Present in the following documents:
  • Main text
View BVdb publication page