Gene
DALRD3
DALR anticodon binding domain containing 3
- HGNC 25536↗(opens in a new tab)
- Ensembl gene ENSG00000178149↗(opens in a new tab)
- NCBI Gene 55152↗(opens in a new tab)
Summary
- Cytogenetic location
- 3p21.31
- Coordinates
- Chromosome 3: 49,015,488–49,018,580 (GRCh38)
- Exons
- 12 exons across 3.1 kb
- Protein
- 543 amino acids
- Also known as
- FLJ10496
- MANE Select transcript
- ENST00000341949.9NM_001009996.3
- 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 DALRD3 yet. The test sequences your whole genome, so your data includes it all the same.
How DALRD3 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 1.7 kb of the gene's 3.1 kb; 1,632 of those bases code for the protein.
How a genome test reads DALRD3
1
position in DALRD3 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 3.1 kb of DALRD3, introns included, not only the 1.7 kb of exons.
Traits linked to DALRD3
The Human Phenotype Ontology lists these as features of the rare conditions DALRD3 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Absent speech development
- Dystonia
- Myoclonic seizure
- Severe global developmental delay
- Encephalopathy
- Abnormality of coordination
- CNS hypomyelination
- Decreased reflex response
Show 25 more traits
- Delayed speech and language development
- EEG with multifocal slow activity
- Epilepsy
- Global developmental delay
- Intellectual disability
- Loss of developmental milestones
- Abnormal corpus callosum morphology
- Abnormal gait
- Abnormal myelination
- Ataxia
- Attention deficit
- Autism
- Behavioral abnormality
- Brain degeneration
- Degeneration of cerebrum
- Diminished deep tendon reflex
- Disorder of involuntary muscle movements
- Hypsarrhythmia
- Impulsivity
- Involuntary movements
- Jerking
- Mental deterioration
- Tremor
- Unsteady walk
- Repeated seizures without recovery between them
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.). DALRD3 gene: DALR anticodon binding domain containing 3. Retrieved 16 October 2026, from https://dantelabs.com/genes/dalrd3
Dante Labs. DALRD3 gene: DALR anticodon binding domain containing 3 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/dalrd3
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