Gene
DPYSL5
dihydropyrimidinase like 5
- HGNC 20637↗(opens in a new tab)
- Ensembl gene ENSG00000157851↗(opens in a new tab)
- NCBI Gene 56896↗(opens in a new tab)
Summary
- Cytogenetic location
- 2p23.3
- Coordinates
- Chromosome 2: 26,848,132–26,950,351 (GRCh38)
- Exons
- 13 exons across 102.2 kb
- Protein
- 564 amino acids
- Also known as
- CRMP5, Ulip6, CRMP-5, CRAM, CV2
- MANE Select transcript
- ENST00000288699.11NM_020134.4
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
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No Genome Test report reads DPYSL5 yet. The test sequences your whole genome, so your data includes it all the same.
How DPYSL5 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 5.2 kb of the gene's 102.2 kb; 1,695 of those bases code for the protein.
How a genome test reads DPYSL5
1
position in DPYSL5 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 102.2 kb of DPYSL5, introns included, not only the 5.2 kb of exons.
Traits linked to DPYSL5
The Human Phenotype Ontology lists these as features of the rare conditions DPYSL5 can cause. Each trait's page lists the other genes linked to it.
Abnormality of head or neck
- Abnormal cranial suture/fontanelle morphology
- Dandy-Walker malformation
- Frontal bossing
- Wide nasal bridge
- Big calvaria
- Cleft palate
- Depressed nasal bridge
- Downward slanting of the opening between the eyelids
Show 16 more traits
Abnormality of the nervous system
- Agenesis of corpus callosum
- Delayed ability to sit
- Delayed ability to walk
- Intellectual disability, severe
- Severe global developmental delay
- Abnormal speech pattern
- Global developmental delay
- Intellectual disability
Show 16 more traits
- Small cerebellum
- Absent speech development
- Absent/small cerebellum
- Aggressive behavior
- Ataxia
- Dysgenesis of the hippocampus
- Too much cerebrospinal fluid in the brain
- Ventriculomegaly
- Abnormality of neuronal migration
- Autism spectrum disorder
- Chorea
- Grand mal seizures
- Impulsivity
- Involuntary writhing movements in fingers, hands, toes, and feet
- Repetitive movements
- Seizure affecting one half of brain
Abnormality of the cardiovascular system
- Abnormal mitral valve morphology
- Abnormal tricuspid valve morphology
- An opening in the wall separating the top two chambers of the heart
- Hole in center of heart
- Hole in heart wall separating two lower heart chambers
- Narrowing of aortic valve
- Narrowing of pulmonic valve
- Tetralogy of Fallot
Show 1 more trait
Abnormality of the eye
- Wide-set eyes
- Abnormally close eyes
- Cross-eyed
- Deeply set eye
- Birth defect that causes a hole in the innermost layer at the back of the eye
- Bulging eye
- Cat eye
- Glaucoma
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.). DPYSL5 gene: dihydropyrimidinase like 5. Retrieved 17 October 2026, from https://dantelabs.com/genes/dpysl5
Dante Labs. DPYSL5 gene: dihydropyrimidinase like 5 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/dpysl5
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