Gene
TP53TG3B
TP53 target 3B
- HGNC 37202↗(opens in a new tab)
- Ensembl gene ENSG00000261509↗(opens in a new tab)
- NCBI Gene 729355↗(opens in a new tab)
Summary
- Cytogenetic location
- 16p11.2
- Coordinates
- Chromosome 16: 33,360,841–33,363,478 (GRCh38)
- Exons
- 2 exons across 2.6 kb
- Protein
- 124 amino acids
- MANE Select transcript
- ENST00000341305.7NM_001099687.4
- Locus type
- Protein-coding
- Very high
- Confident
- Low
- Very low
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No Genome Test report reads TP53TG3B yet. The test sequences your whole genome, so your data includes it all the same.
How TP53TG3B 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 1.5 kb of the gene's 2.6 kb; 375 of those bases code for the protein.
Sequencing TP53TG3B
100Hard
How hard TP53TG3B is to sequence with short reads, out of 100
0 · Easy100 · Hard
Much of TP53TG3B sits where short reads can miss or misplace a change.
What adds to it: the share of TP53TG3B'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 100.100%
- 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 60.100%
- 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 30.2.9%
- 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 20.0%
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 TP53TG3B'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
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.
- The Genome in a Bottle genome stratifications, from NIST: the sequencing difficulty score.
Cite this page
Dante Labs. (n.d.). TP53TG3B gene: TP53 target 3B. Retrieved 20 October 2026, from https://dantelabs.com/genes/tp53tg3b
Dante Labs. TP53TG3B gene: TP53 target 3B [Internet]. [cited 20 October 2026]. Available from: https://dantelabs.com/genes/tp53tg3b
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