GNB1L c.*5042C>T

Variant ID: 22-19771190-G-A

NM_053004.2(GNB1L):c.*5042C>T

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Molecular mechanisms in 22q11 deletion syndrome.

Schizophrenia Bulletin
Williams, Nigel M NM
Publication Date: 2011-09

Variant appearance in text: rs5746832
PubMed Link: 21860033
Variant Present in the following documents:
  • Main text
View BVdb publication page



Supportive evidence for reduced expression of GNB1L in schizophrenia.

Schizophrenia Bulletin
Ishiguro, Hiroki H; Koga, Minori M; Horiuchi, Yasue Y; Noguchi, Emiko E; Morikawa, Miyuki M; Suzuki, Yoshimi Y; Arai, Makoto M; Niizato, Kazuhiro K; Iritani, Shyuji S; Itokawa, Masanari M; Inada, Toshiya T; Iwata, Nakao N; Ozaki, Norio N; Ujike, Hiroshi H; Kunugi, Hiroshi H; Sasaki, Tsukasa T; Takahashi, Makoto M; Watanabe, Yuichiro Y; Someya, Toshiyuki T; Kakita, Akiyoshi A; Takahashi, Hitoshi H; Nawa, Hiroyuki H; Arinami, Tadao T
Publication Date: 2010-07

Variant appearance in text: rs5746832
PubMed Link: 19011233
Variant Present in the following documents:
  • Main text
View BVdb publication page