Gene
NYNRIN
NYN domain and retroviral integrase containing
- HGNC 20165↗(opens in a new tab)
- Ensembl gene ENSG00000205978↗(opens in a new tab)
- NCBI Gene 57523↗(opens in a new tab)
Summary
- Cytogenetic location
- 14q12
- Coordinates
- Chromosome 14: 24,399,003–24,419,283 (GRCh38)
- Exons
- 9 exons across 20.3 kb
- Protein
- 1,898 amino acids
- Also known as
- FLJ11811, CGIN1
- Previous symbols
- KIAA1305
- MANE Select transcript
- ENST00000382554.4NM_025081.3
- Locus type
- Protein-coding
- Very high
- Confident
- Low
- Very low
This page as data
Add .json to the page's address, or ask for application/json, to read it as JSON.
library(jsonlite)
url <- "https://dantelabs.com/genes/nynrin.json"
page <- fromJSON(url)
page$gene$nameRead NYNRIN, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated reports relevant to this gene
No Genome Test report reads NYNRIN yet. The test sequences your whole genome, so your data includes it all the same.
How NYNRIN is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
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 7.6 kb of the gene's 20.3 kb; 5,697 of those bases code for the protein.
Sequencing NYNRIN
3Easy
How hard NYNRIN is to sequence with short reads, out of 100
0 · Easy100 · Hard
Almost all of NYNRIN's exons sit where short reads map cleanly.
What adds to it: the share of NYNRIN'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. Weight 100%.0%
- HomologySegmental duplications: copies elsewhere in the genome, such as paralogues and pseudogenes, at 90% identity or more. Weight 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 reads from either may land on the other. Weight 60%.0%
- Reference coverageGaps in the reference assembly nearby, where there is no sequence for reads to align to. Weight 50%.0%
- RepeatsTandem repeats and runs of one base, which reads slip on and may not span. Weight 30%.2.4%
- GC contentWindows under 25% or over 65% G and C, which library preparation covers thinly. Weight 20%.12%
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 NYNRIN'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
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.). NYNRIN gene: NYN domain and retroviral integrase containing. Retrieved 19 October 2026, from https://dantelabs.com/genes/nynrin
Dante Labs. NYNRIN gene: NYN domain and retroviral integrase containing [Internet]. [cited 19 October 2026]. Available from: https://dantelabs.com/genes/nynrin
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks