Canonical-transcript structure of the two partner genes, and the read-level evidence
supporting the fusion in each tumor sample.
Known studies
Recorded in the Mitelman Database of Chromosome
Aberrations and Gene Fusions in Cancer in 4 publications (17 reported cases). Reported in:
Adenocarcinoma; Malignant epithelial tumor, special type; Nonneoplastic mesenchymal disorder/lesion; Nonneoplastic hematologic disorder/lesion; Nonneoplastic epithelial disorder/lesion; Schwannoma.
Fu et al 2024,
Biomark Res — Adenocarcinoma; Malignant epithelial tumor, special type (Oesophagus)
Lai et al 2015,
BMC Genomics — Adenocarcinoma (Prostate)
Canonical transcripts shown in genomic order
on chr1 (lower-coordinate gene on the left). Each gene is drawn at its own zoom level. Introns are compressed
to 1% of their genomic length so the exons are easier to see — the
pixel-space x-axis is therefore non-linear, but the labelled start and
end coordinates of each transcript are exact. The gap shown between
the two panels (when on the same chromosome) is the actual distance
between gene bodies. Transcript IDs are MANE Select where available,
else Ensembl_canonical, else the longest protein-coding transcript.