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UNC5B c.1282_1283delinsGA ;(p.T428E)
Variant ID: 10-73050854-AC-GA
NM_170744.4(
UNC5B
):c.1282_1283delinsGA;(p.T428E)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Netrin1 deficiency activates MST1 via UNC5B receptor, promoting dopaminergic apoptosis in Parkinson's disease.
Proceedings Of The National Academy Of Sciences Of The United States Of America
Ahn, Eun Hee EH; Kang, Seong Su SS; Qi, Qi Q; Liu, Xia X; Ye, Keqiang K
Publication Date: 2020-09-29
Variant appearance in text: UNC5B: T428E
PubMed Link:
32929029
Variant Present in the following documents:
Main text
View BVdb publication page