Gene
NDE1
nudE neurodevelopment protein 1
- HGNC 17619↗(opens in a new tab)
- Ensembl gene ENSG00000072864↗(opens in a new tab)
- NCBI Gene 54820↗(opens in a new tab)
Summary
- Cytogenetic location
- 16p13.11
- Coordinates
- Chromosome 16: 15,650,245–15,726,353 (GRCh38)
- Exons
- 9 exons across 76.1 kb
- Protein
- 335 amino acids
- Also known as
- nudE, FLJ20101, NDE
- MANE Select transcript
- ENST00000396354.6NM_017668.3
- 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 NDE1 yet. The test sequences your whole genome, so your data includes it all the same.
How NDE1 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 3.2 kb of the gene's 76.1 kb; 1,008 of those bases code for the protein.
How a genome test reads NDE1
7
positions in NDE1 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 76.1 kb of NDE1, introns included, not only the 3.2 kb of exons.
Traits linked to NDE1
The Human Phenotype Ontology lists these as features of the rare conditions NDE1 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the nervous system
- Agenesis of corpus callosum
- Global developmental delay
- Increased reflexes
- Intellectual disability, severe
- IQ less than 20
- Poor eye contact
- Self-mutilation
- Small brainstem
Show 26 more traits
- Small cerebellum
- Ventriculomegaly
- 4-layered lissencephaly
- Abnormal corpus striatum morphology
- Decrease in size of the outer layer of the brain due to loss of brain cells
- Intellectual disability
- Microlissencephaly
- Simplified gyral pattern
- Abnormal dura mater morphology
- Babinski sign
- Colpocephaly
- Dysgenesis of the thalamus
- Epilepsy
- Fewer or absent grooves in brain
- Lethargy
- Profound global developmental delay
- Severe global developmental delay
- Small hippocampus
- Thalamic edema
- Abnormality of neuronal migration
- Degeneration of cerebellum
- Underdevelopment of part of brain called corpus callosum
- Fewer and broader ridges in brain
- Generalized myoclonic seizure
- Hydranencephaly
- Involuntary writhing movements in fingers, hands, toes, and feet
Abnormality of the musculoskeletal system
- Diffuse skeletal muscle wasting
- Poor head control
- Spastic tetraplegia
- Abnormal muscle tone
- Opisthotonus
- Spastic diplegia
- Spasticity and rigidity of muscles
- Abnormal deposits of calcium in the brain
Show 2 more traits
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.). NDE1 gene: nudE neurodevelopment protein 1. Retrieved 16 October 2026, from https://dantelabs.com/genes/nde1
Dante Labs. NDE1 gene: nudE neurodevelopment protein 1 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/nde1
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