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RPL29P28::RPL29

High support

Canonical-transcript structure of the two partner genes, and the read-level evidence supporting the fusion in each tumor sample.

Known studies

No published studies in the Mitelman database describe the RPL29P28::RPL29 gene fusion. It may be novel, private to this case, or a technical artifact — absence from a curated database is not by itself evidence either way.

Canonical transcripts in genomic order spliced together in the fusion mRNA chr13 RPL29P28 (-) ENST00000421928 · Ensembl canonical 36,926,530 breakpoint 36,926,438 36,927,219 2 exons · 781 bp chr3 RPL29 (-) ENST00000294189 · Ensembl canonical 51,993,865 breakpoint 51,993,522 51,995,895 4 exons · 2.4 kb
Canonical transcripts shown in genomic order — RPL29P28 on chr13, RPL29 on chr3. 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.

Left hand (primary)

Reportable 94 fragments (1 split, 0 discordant) · RPL29P28 exon 2 → RPL29 exon 4

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