Gene
USP9Y
ubiquitin specific peptidase 9 Y-linked
- HGNC 12633↗(opens in a new tab)
- Ensembl gene ENSG00000114374↗(opens in a new tab)
- NCBI Gene 8287↗(opens in a new tab)
Summary
- Cytogenetic location
- Yq11.221
- Coordinates
- Chromosome Y: 12,701,231–12,860,839 (GRCh38)
- Exons
- 46 exons across 159.6 kb
- Protein
- 2,555 amino acids
- Also known as
- DFFRY, FAF-Y, AZFA
- MANE Select transcript
- ENST00000338981.7NM_004654.4
- 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/usp9y.json"
page <- fromJSON(url)
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No Genome Test report reads USP9Y yet. The test sequences your whole genome, so your data includes it all the same.
How USP9Y is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- 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 10 kb of the gene's 159.6 kb; 7,668 of those bases code for the protein.
Sequencing USP9Y
1Low
How hard USP9Y is to sequence with short reads, out of 100Each bar is the share of USP9Y's exon bases in that kind of difficult region. The score weighs them by how much each costs a short-read call: 0 when no base is in any, 100 when every base is in all of them.
- MappabilityStretches where 100 or 250 bp reads cannot be placed uniquely, so a call there may be missing or wrong. Weight 35%.0%
- HomologySegmental duplications: copies elsewhere in the genome, such as paralogues and pseudogenes, at 90% identity or more. Weight 30%.0%
- RepeatsTandem repeats and runs of one base, which reads slip on and may not span. Weight 15%.2.4%
- GC contentWindows under 25% or over 65% G and C, which library preparation covers thinly. Weight 10%.4.6%
- Reference coverageGaps in the reference assembly nearby, where there is no sequence for reads to align to. Weight 10%.0%
1
position in USP9Y 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 159.6 kb of USP9Y, introns included, not only the 10 kb of exons.
Traits linked to USP9Y
The Human Phenotype Ontology lists these as features of the rare conditions USP9Y can cause. Each trait's page lists the other genes linked to it.
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.
- The Genome in a Bottle genome stratifications, from NIST: the sequencing difficulty score.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.17-8666dff2.
Cite this page
Dante Labs. (n.d.). USP9Y gene: ubiquitin specific peptidase 9 Y-linked. Retrieved 17 October 2026, from https://dantelabs.com/genes/usp9y
Dante Labs. USP9Y gene: ubiquitin specific peptidase 9 Y-linked [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/usp9y
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