Gene
TFPT
TCF3 fusion partner
- HGNC 13630↗(opens in a new tab)
- Ensembl gene ENSG00000105619↗(opens in a new tab)
- NCBI Gene 29844↗(opens in a new tab)
Summary
- Cytogenetic location
- 19q13.42
- Coordinates
- Chromosome 19: 54,107,020–54,115,657 (GRCh38)
- Exons
- 6 exons across 8.6 kb
- Protein
- 253 amino acids
- Also known as
- FB1, amida, INO80F
- MANE Select transcript
- ENST00000391759.6NM_013342.4
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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No Genome Test report reads TFPT yet. The test sequences your whole genome, so your data includes it all the same.
How TFPT is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 1.2 kb of the gene's 8.6 kb; 762 of those bases code for the protein.
How a genome test reads TFPT
1
position in TFPT where ClinVar classes a change as pathogenic or likely pathogenic
None of them falls in a region short reads find hard.
A whole genome covers all 8.6 kb of TFPT, introns included, not only the 1.2 kb of exons.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). TFPT gene: TCF3 fusion partner. Retrieved 17 October 2026, from https://dantelabs.com/genes/tfpt
Dante Labs. TFPT gene: TCF3 fusion partner [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/tfpt
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