Gene
C17orf107
chromosome 17 open reading frame 107
- HGNC 37238↗(opens in a new tab)
- Ensembl gene ENSG00000205710↗(opens in a new tab)
- NCBI Gene 100130311↗(opens in a new tab)
Summary
- Cytogenetic location
- 17p13.2
- Coordinates
- Chromosome 17: 4,899,536–4,902,934 (GRCh38)
- Exons
- 3 exons across 3.4 kb
- Protein
- 190 amino acids
- MANE Select transcript
- ENST00000381365.4NM_001145536.2
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
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No Genome Test report reads C17orf107 yet. The test sequences your whole genome, so your data includes it all the same.
How C17orf107 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
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 3.2 kb of the gene's 3.4 kb; 573 of those bases code for the protein.
How a genome test reads C17orf107
3
positions in C17orf107 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 3.4 kb of C17orf107, introns included, not only the 3.2 kb of exons.
External links
Gene records
Transcript
Protein
Clinical
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.). C17orf107 gene: chromosome 17 open reading frame 107. Retrieved 17 October 2026, from https://dantelabs.com/genes/c17orf107
Dante Labs. C17orf107 gene: chromosome 17 open reading frame 107 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/c17orf107
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