Gene
TRIM8
tripartite motif containing 8
- HGNC 15579↗(opens in a new tab)
- Ensembl gene ENSG00000171206↗(opens in a new tab)
- NCBI Gene 81603↗(opens in a new tab)
Summary
- Cytogenetic location
- 10q24.32
- Coordinates
- Chromosome 10: 102,644,479–102,658,318 (GRCh38)
- Exons
- 6 exons across 13.8 kb
- Protein
- 551 amino acids
- Also known as
- GERP
- Previous symbols
- RNF27
- MANE Select transcript
- ENST00000643721.2NM_030912.3
- 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/trim8.json"
page <- fromJSON(url)
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No Genome Test report reads TRIM8 yet. The test sequences your whole genome, so your data includes it all the same.
How TRIM8 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
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 2.8 kb of the gene's 13.8 kb; 1,656 of those bases code for the protein.
Sequencing TRIM8
14
positions in TRIM8 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 13.8 kb of TRIM8, introns included, not only the 2.8 kb of exons.
Traits linked to TRIM8
The Human Phenotype Ontology lists these as features of the rare conditions TRIM8 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Delayed ability to walk
- EEG with occipital epileptiform discharges
- EEG with parietal epileptiform discharges
- Epilepsy
- Global developmental delay
- Hypsarrhythmia
- Intellectual disability, severe
- No social interaction
Show 51 more traits
- Poor eye contact
- Severe global developmental delay
- Absent speech development
- Epileptic encephalopathy
- Focal motor seizure
- Generalized myoclonic seizure
- Intellectual disability
- Ataxia
- Delayed ability to sit
- Delayed CNS myelination
- Difficulty sleeping
- EEG abnormality
- EEG with burst suppression
- Focal tonic seizure
- Grand mal seizures
- Increased reflexes
- Lethargy
- Atypical absence seizure
- Autism spectrum disorder
- Bilateral tonic-clonic seizure with focal onset
- Brief seizures with staring spells
- Choreoathetosis
- Continuous spike and waves during slow sleep
- Decrease in size of the outer layer of the brain due to loss of brain cells
- Decreased reflex response
- Degeneration of cerebellum
- Delayed myelination
- Diffuse cerebral atrophy
- Diffuse white matter abnormalities
- Disorder of involuntary muscle movements
- EEG with spike-wave complexes
- Episodic ataxia
- Febrile seizure (within the age range of 3 months to 6 years)
- Fewer and broader ridges in brain
- Focal impaired awareness seizure
- Generalized clonic seizure
- Generalized tonic seizure
- Head tremor
- Infantile spasms
- Jerking
- Loss of developmental milestones
- More active than typical
- Repetitive movements
- Seizure affecting one half of brain
- Self-injurious behavior
- Sudden loss of muscle tone
- Tonic seizure
- Tremor
- Underdevelopment of part of brain called corpus callosum
- Uni- and bilateral multifocal epileptiform discharges
- Dystonia
Abnormality of head or neck
- Abnormally small head
- Long philtrum
- Monobrow
- Gum enlargement
- Smooth philtrum
- Cleft palate
- Depressed nasal bridge
- Nasal tip, upturned
Show 1 more trait
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.). TRIM8 gene: tripartite motif containing 8. Retrieved 17 October 2026, from https://dantelabs.com/genes/trim8
Dante Labs. TRIM8 gene: tripartite motif containing 8 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/trim8
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