Bibliome.ai browser hg19
Search
About
Stats
FAQ
NR0B2 c.46_47delinsGA ;(p.S16D)
Variant ID: 1-27240385-CT-TC
NM_021969.2(
NR0B2
):c.46_47delinsGA;(p.S16D)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Hepatocellular cystathionine γ lyase/hydrogen sulfide attenuates nonalcoholic fatty liver disease by activating farnesoid X receptor.
Hepatology (Baltimore, Md.)
Xu, Wenjing W; Cui, Changting C; Cui, Chunmei C; Chen, Zhenzhen Z; Zhang, Haizeng H; Cui, Qinghua Q; Xu, Guoheng G; Fan, Jianglin J; Han, Yu Y; Tang, Liangjie L; Targher, Giovanni G; Byrne, Christopher D CD; Zheng, Ming-Hua MH; Yang, Liming L; Cai, Jun J; Geng, Bin B
Publication Date: 2022-12
Variant appearance in text: SHP: S16D
PubMed Link:
35586979
Variant Present in the following documents:
Main text
HEP-76-1794.pdf
View BVdb publication page
Spatial phylogenetics of Japanese ferns: Patterns, processes, and implications for conservation.
American Journal Of Botany
Nitta, Joel H JH; Mishler, Brent D BD; Iwasaki, Wataru W; Ebihara, Atsushi A
Publication Date: 2022-05
Variant appearance in text: SHP: S16D
PubMed Link:
35435239
Variant Present in the following documents:
Main text
AJB2-109-727.pdf
View BVdb publication page