Gene
NEK2
NIMA related kinase 2
- HGNC 7745↗(opens in a new tab)
- Ensembl gene ENSG00000117650↗(opens in a new tab)
- NCBI Gene 4751↗(opens in a new tab)
Summary
- Cytogenetic location
- 1q32.3
- Coordinates
- Chromosome 1: 211,662,772–211,675,621 (GRCh38)
- Exons
- 8 exons across 12.9 kb
- Protein
- 445 amino acids
- Also known as
- NLK1, NEK2A, RP67, PPP1R111
- MANE Select transcript
- ENST00000366999.9NM_002497.4
- 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.
Read NEK2, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated reports relevant to this gene
No Genome Test report reads NEK2 yet. The test sequences your whole genome, so your data includes it all the same.
How NEK2 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 2.1 kb of the gene's 12.9 kb; 1,338 of those bases code for the protein.
How a genome test reads NEK2
6
positions in NEK2 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 12.9 kb of NEK2, introns included, not only the 2.1 kb of exons.
Traits linked to NEK2
The Human Phenotype Ontology lists these as features of the rare conditions NEK2 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the eye
- Rod-cone dystrophy
- Abnormal electroretinogram
- Abnormal retinal pigmentation
- Blindness
- Extreme sensitivity of the eyes to light
- Involuntary, rapid, rhythmic eye movements
- Optic atrophy
- Progressive night blindness
Show 19 more traits
- Retina degeneration
- Spicular pigmentation of the retina
- Visual impairment
- Abnormal central response of multifocal electroretinogram
- Abnormal full-field electroretinogram
- Bulging cornea
- Cystoid macular edema
- Difficulties with night vision
- Eye muscle paralysis
- Glaucoma
- Loss of peripheral vision
- Optic disc drusen
- Optic disc pallor
- Photoreceptor outer segment loss on macular OCT
- Posterior subcapsular cataract
- Retinal atrophy
- Abnormal color vision
- Decreased clarity of vision
- Photopsia
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.). NEK2 gene: NIMA related kinase 2. Retrieved 17 October 2026, from https://dantelabs.com/genes/nek2
Dante Labs. NEK2 gene: NIMA related kinase 2 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/nek2
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks