Gene
USP7
ubiquitin specific peptidase 7
- HGNC 12630↗(opens in a new tab)
- Ensembl gene ENSG00000187555↗(opens in a new tab)
- NCBI Gene 7874↗(opens in a new tab)
Summary
- Cytogenetic location
- 16p13.2
- Coordinates
- Chromosome 16: 8,892,097–8,963,906 (GRCh38)
- Exons
- 31 exons across 71.8 kb
- Protein
- 1,102 amino acids
- Previous symbols
- HAUSP
- MANE Select transcript
- ENST00000344836.9NM_003470.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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No Genome Test report reads USP7 yet. The test sequences your whole genome, so your data includes it all the same.
How USP7 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 5.8 kb of the gene's 71.8 kb; 3,309 of those bases code for the protein.
How a genome test reads USP7
17
positions in USP7 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 71.8 kb of USP7, introns included, not only the 5.8 kb of exons.
Traits linked to USP7
The Human Phenotype Ontology lists these as features of the rare conditions USP7 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Delayed speech and language development
- Global developmental delay
- Intellectual disability
- Brain imaging abnormality
- Abnormal gait
- Aggressive behavior
- Apraxia
- Attention deficit
Show 18 more traits
- Autism spectrum disorder
- Cerebral white matter atrophy
- Dilated third ventricle
- Epilepsy
- Underdevelopment of part of brain called corpus callosum
- Abnormal temper tantrums
- Absent speech development
- Difficulty sleeping
- Impulsivity
- Obsessive-compulsive trait
- Pauses in breathing while sleeping
- Periventricular leukomalacia
- Skin-picking
- Too much cerebrospinal fluid in the brain
- Ventriculomegaly
- Central sleep apnea
- Perseverative thought
- Speech apraxia
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 Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). USP7 gene: ubiquitin specific peptidase 7. Retrieved 17 October 2026, from https://dantelabs.com/genes/usp7
Dante Labs. USP7 gene: ubiquitin specific peptidase 7 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/usp7
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