Bibliome.ai browser hg19
Search
About
Stats
FAQ
PPP1R3F c.1004+3495C>T
Variant ID: X-49130831-C-T
NM_033215.4(
PPP1R3F
):c.1004+3495C>T
This variant was identified in 7 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
The association of FOXP3 gene polymorphisms with cancer susceptibility: a comprehensive systemic review and meta-analysis.
Bioscience Reports
Chen, Yan Y; Qi, Xiaoxue X; Bian, Ce C; Ling, Chen C; Yi, Tao T; Mu, Xiyan X; Zhao, Xia X
Publication Date: 2019-03-29
Variant appearance in text: rs5906761
PubMed Link:
30782783
Variant Present in the following documents:
Main text
bsr-39-bsr20181809.pdf
View BVdb publication page
Regulatory T Cell and Forkhead Box Protein 3 as Modulators of Immune Homeostasis.
Frontiers In Immunology
Pereira, Leonn Mendes Soares LMS; Gomes, Samara Tatielle Monteiro STM; Ishak, Ricardo R; Vallinoto, Antonio Carlos Rosário ACR
Publication Date: 2017
Variant appearance in text: rs5906761
PubMed Link:
28603524
Variant Present in the following documents:
Main text
fimmu-08-00605.pdf
View BVdb publication page
Genetic and epigenetic studies of FOXP3 in asthma and allergy.
Asthma Research And Practice
Marques, Cintia Rodrigues CR; Costa, Ryan Santos RS; Costa, Gustavo Nunes de Oliveira GNO; da Silva, Thiago Magalhães TM; Teixeira, Tatiane Oliveira TO; de Andrade, Emília Maria Medeiros EMM; Galvão, Alana A AA; Carneiro, Valdirene Leão VL; Figueiredo, Camila Alexandrina CA
Publication Date: 2015
Variant appearance in text: rs5906761
PubMed Link:
27965764
Variant Present in the following documents:
Main text
40733_2015_Article_12.pdf
View BVdb publication page
Association signals unveiled by a comprehensive gene set enrichment analysis of dental caries genome-wide association studies.
Plos One
Wang, Quan Q; Jia, Peilin P; Cuenco, Karen T KT; Zeng, Zhen Z; Feingold, Eleanor E; Marazita, Mary L ML; Wang, Lily L; Zhao, Zhongming Z
Publication Date: 2013
Variant appearance in text: rs5906761
PubMed Link:
23967329
Variant Present in the following documents:
Main text
pone.0072653.pdf
View BVdb publication page
Intron-1 rs3761548 is related to the defective transcription of Foxp3 in psoriasis through abrogating E47/c-Myb binding.
Journal Of Cellular And Molecular Medicine
Shen, Z Z; Chen, L L; Hao, F F; Wang, G G; Liu, Y Y
Publication Date: 2010-01
Variant appearance in text: rs5906761
PubMed Link:
20414968
Variant Present in the following documents:
Main text
View BVdb publication page
Overview of the Rapid Response data.
Genes And Immunity
Brown, W M WM; Pierce, J J JJ; Hilner, J E JE; Perdue, L H LH; Lohman, K K; Lu, L L; de Bakker, P I W PI; Irenze, K K; Ziaugra, L L; Mirel, D B DB; ,
Publication Date: 2009-12
Variant appearance in text: rs5906761
PubMed Link:
19956101
Variant Present in the following documents:
Main text
View BVdb publication page
SNPs in the FOXP3 gene region show no association with Juvenile Idiopathic Arthritis in a UK Caucasian population.
Rheumatology (Oxford, England)
Eastell, T T; , ; Hinks, A A; Thomson, W W
Publication Date: 2007-08
Variant appearance in text: rs5906761
PubMed Link:
17526924
Variant Present in the following documents:
Main text
View BVdb publication page