Colorectal cancer (CRC) (primary tumor sample and matched adjacent tissues) |
VTI1A-TCF7L2 gene fusion |
Bass et al., 2011 |
CRC cell lines and tissues |
Splice variants of VTI1A-TCF7L2 fusion transcripts |
Nome et al., 2014 |
CRC genome wide association studies (GWAS) |
Risk locus at 10q25 (rs12241008, intronic to VTI1A) |
Wang et al., 2014 |
Non-small cell lung cancer association |
Allele A of VTI1A SNP rs7086803 |
Su et al., 2015 |
Glioma GWAS |
Risk locus at 10q25.2 (rs11196067), near the VTI1A gene locus |
Kinnersley et al., 2015 |
CRC GWAS |
Risk locus at 10q25.2 (rs10506868) |
Zeng et al., 2016 |
Glioma association |
Risk locus rs11196067 |
Wang et al., 2017a, Wang et al., 2017b
|
Associations between variants in the VTI1A-TCF7L2 region and cancer susceptibility |
8 common variants of VTI1A and TCF7L2 associated with various cancers |
Zhang et al., 2018 |
Hepatocellular carcinoma (HCC) RNA sequencing |
VTI1A-CFAP46 fusion transcript (from a genomic DNA VTI1A-CFAP46 translocation event) |
Tsuge et al., 2019 |
Non-small-cell lung adenocarcinoma, whole-transcriptome sequencing |
VAMP2-NRG1 gene fusion |
Jung et al., 2015 |
Gastrointestinal stromal tumors, exome and transciptome sequencing |
STX16-NPEPL1 gene fusion |
Kang et al., 2016 |