Gene
PTCSC3
papillary thyroid carcinoma susceptibility candidate 3
- HGNC 43959↗(opens in a new tab)
- Ensembl gene ENSG00000259104↗(opens in a new tab)
- NCBI Gene 100886964↗(opens in a new tab)
Summary
- Cytogenetic location
- 14q13.3
- Coordinates
- Chromosome 14: 36,134,890–36,176,722 (GRCh38)
- Exons
- 4 exons across 41.8 kb
- MANE Select transcript
- ENST00000556013.4NR_049735.3
- Locus type
- Long non-coding RNA (lncRNA)
This page as data
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No Genome Test report reads PTCSC3 yet. The test sequences your whole genome, so your data includes it all the same.
How PTCSC3 is laid out
- 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 2 kb of the gene's 41.8 kb.
Sequencing PTCSC3
3Easy
How hard PTCSC3 is to sequence with short reads, out of 100
0 · Easy100 · Hard
Almost all of PTCSC3's exons sit where short reads map cleanly.
What adds to it: the share of PTCSC3's exons in each kind of hard region
- MappabilityStretches where 100 or 250 bp reads cannot be placed uniquely, so a call there may be missing or wrong. On its own, a gene wholly in this kind of region would score 100.1.4%
- HomologySegmental duplications: copies elsewhere in the genome, such as paralogues and pseudogenes, at 90% identity or more. On its own, a gene wholly in this kind of region would score 60.0%
- Shared with chrYThe pseudoautosomal regions and the X-transposed region, where chrX and chrY carry the same or nearly the same sequence, so a read from one may be placed on the other. On its own, a gene wholly in this kind of region would score 60.0%
- Reference coverageGaps in the reference assembly nearby, where there is no sequence for reads to align to. On its own, a gene wholly in this kind of region would score 50.0%
- RepeatsTandem repeats and runs of one base, which reads slip on and may not span. On its own, a gene wholly in this kind of region would score 30.6.3%
- GC contentWindows under 25% or over 65% G and C, which library preparation covers thinly. On its own, a gene wholly in this kind of region would score 20.1.4%
A Dante Labs score from our own research, built on NIST's Genome in a Bottle maps of hard-to-sequence regions.How it's scoredEach bar is the share of PTCSC3's exon bases in that kind of difficult region. Any one kind can make a gene hard on its own, and each further kind adds less: 0 when no base is in any, 100 when every base is where reads cannot be placed uniquely.
External links
Gene records
Transcript
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.
- The Genome in a Bottle genome stratifications, from NIST: the sequencing difficulty score.
Cite this page
Dante Labs. (n.d.). PTCSC3 gene: papillary thyroid carcinoma susceptibility candidate 3. Retrieved 20 October 2026, from https://dantelabs.com/genes/ptcsc3
Dante Labs. PTCSC3 gene: papillary thyroid carcinoma susceptibility candidate 3 [Internet]. [cited 20 October 2026]. Available from: https://dantelabs.com/genes/ptcsc3
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