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PRRT2 c.499_500delinsGA ;(p.T167D)
Variant ID: 16-29824874-AC-GA
NM_145239.2(
PRRT2
):c.499_500delinsGA;(p.T167D)
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:
A phosphorylation-deficient mutant of retinoid X receptor α at Thr 167 alters fasting response and energy metabolism in mice.
Laboratory Investigation; A Journal Of Technical Methods And Pathology
Sueyoshi, Tatsuya T; Sakuma, Tsutomu T; Shindo, Sawako S; Fashe, Muluneh M; Kanayama, Tomohiko T; Ray, Manas M; Moore, Rick R; Negishi, Masahiko M
Publication Date: 2019-10
Variant appearance in text: PKC: T167D
PubMed Link:
31152145
Variant Present in the following documents:
Main text
View BVdb publication page