PLXNA2 c.2857-101C>T

Variant ID: 1-208225909-G-A

NM_025179.3(PLXNA2):c.2857-101C>T

This variant was identified in 8 publications

View GRCh38 version.




Publications:


JAK-STAT signaling in inflammatory breast cancer enables chemotherapy-resistant cell states.

Cancer Research
Stevens, Laura E LE; Peluffo, Guillermo G; Qiu, Xintao X; Temko, Daniel D; Fassl, Anne A; Li, Zheqi Z; Trinh, Anne A; Seehawer, Marco M; Jovanovic, Bojana B; Aleckovic, Masa M; Wilde, Callahan M CM; Geck, Renee C RC; Shu, Shaokun S; Kingston, Natalie L NL; Harper, Nicholas W NW; Almendro, Vanessa V; Pyke, Alanna L AL; Egri, Shawn B SB; Papanastasiou, Malvina M; Clement, Kendell K; Zhou, Ningxuan N; Walker, Sarah S; Salas, Jacqueline J; Park, So Yeon SY; Frank, David A DA; Meissner, Alexander A; Jaffe, Jacob D JD; Sicinski, Piotr P; Toker, Alex A; Michor, Franziska F; Long, Henry W HW; Overmoyer, Beth A BA; Polyak, Kornelia K
Publication Date: 2022-11-21

Variant appearance in text: PLXNA2: 2857-101C>T; rs841865
PubMed Link: 36409824
Variant Present in the following documents:
  • can-22-0423_supplementary_table_s3_suppst3.xlsx, sheet 1
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs841865
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: PLXNA2: 2857-101C>T; rs841865
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_6.xlsx, sheet 1
  • Table_7.xlsx, sheet 1
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs841865
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Cholecystokinin A receptor (CCKAR) gene variation is associated with language lateralization.

Plos One
Ocklenburg, Sebastian S; Arning, Larissa L; Gerding, Wanda M WM; Epplen, Jörg T JT; Güntürkün, Onur O; Beste, Christian C
Publication Date: 2013

Variant appearance in text: rs841865
PubMed Link: 23341962
Variant Present in the following documents:
  • Main text
  • pone.0053643.pdf
View BVdb publication page



Paradox of schizophrenia genetics: is a paradigm shift occurring?

Behavioral And Brain Functions : Bbf
Doi, Nagafumi N; Hoshi, Yoko Y; Itokawa, Masanari M; Yoshikawa, Takeo T; Ichikawa, Tomoe T; Arai, Makoto M; Usui, Chie C; Tachikawa, Hirokazu H
Publication Date: 2012-05-31

Variant appearance in text: rs841865
PubMed Link: 22650965
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mutation of Semaphorin-6A disrupts limbic and cortical connectivity and models neurodevelopmental psychopathology.

Plos One
Rünker, Annette E AE; O'Tuathaigh, Colm C; Dunleavy, Mark M; Morris, Derek W DW; Little, Graham E GE; Corvin, Aiden P AP; Gill, Michael M; Henshall, David C DC; Waddington, John L JL; Mitchell, Kevin J KJ
Publication Date: 2011

Variant appearance in text: rs841865
PubMed Link: 22132072
Variant Present in the following documents:
View BVdb publication page



No association between schizophrenia and polymorphisms of the PlexinA2 gene in Chinese Han Trios.

Schizophrenia Research
Budel, Stephane S; Shim, Sang-Ohk SO; Feng, Zeny Z; Zhao, Hongyu H; Hisama, Fuki F; Strittmatter, Stephen M SM
Publication Date: 2008-02

Variant appearance in text: rs841865
PubMed Link: 18096369
Variant Present in the following documents:
  • Main text
View BVdb publication page