Gene
ZNF408
zinc finger protein 408
- HGNC 20041↗(opens in a new tab)
- Ensembl gene ENSG00000175213↗(opens in a new tab)
- NCBI Gene 79797↗(opens in a new tab)
Summary
- Cytogenetic location
- 11p11.2
- Coordinates
- Chromosome 11: 46,701,031–46,705,912 (GRCh38)
- Exons
- 5 exons across 4.9 kb
- Protein
- 720 amino acids
- Also known as
- FLJ12827, PRDM17
- MANE Select transcript
- ENST00000311764.3NM_024741.3
- 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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Get my Genome TestCurated reports relevant to this gene
Vitreoretinopathy
- Vitreoretinal Degeneration
- 3 GenCC submitters rate it definitive or strong
Broader groupings
Retinitis Pigmentosa
One of 77 genes linked to it
A group of inherited retinal dystrophies with progressive loss of rod and then cone photoreceptors, causing night blindness and gradual loss of peripheral vision.
- 3 GenCC submitters rate it definitive or strong
How ZNF408 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 2.2 kb of the gene's 4.9 kb; 2,163 of those bases code for the protein.
How a genome test reads ZNF408
6
positions in ZNF408 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 4.9 kb of ZNF408, introns included, not only the 2.2 kb of exons.
Genes linked to the same conditions
- BEST1bestrophin 1Shares 2 conditions
- NR2E3nuclear receptor subfamily 2 group E member 3Shares 2 conditions
- NRLneural retina leucine zipperShares 2 conditions
- ABCA4ATP binding cassette subfamily A member 4Shares 1 condition
- AGBL5AGBL carboxypeptidase 5Shares 1 condition
- AHRaryl hydrocarbon receptorShares 1 condition
- ARHGEF18Rho/Rac guanine nucleotide exchange factor 18Shares 1 condition
- ARL2BPARF like GTPase 2 binding proteinShares 1 condition
- ARL3ARF like GTPase 3Shares 1 condition
- ARL6ARF like GTPase 6Shares 1 condition
- BBS2Bardet-Biedl syndrome 2Shares 1 condition
- CA4carbonic anhydrase 4Shares 1 condition
Traits linked to ZNF408
The Human Phenotype Ontology lists these as features of the rare conditions ZNF408 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the eye
- Decreased clarity of vision
- Difficulties with night vision
- Exudative vitreoretinopathy
- Limited peripheral vision
- Optic disc pallor
- Posterior subcapsular cataract
- Rod-cone dystrophy
- Spicular pigmentation of the retina
Show 47 more traits
- Vitreoretinopathy
- Abnormal electroretinogram
- Abnormal retinal pigmentation
- Blindness
- Extreme sensitivity of the eyes to light
- Involuntary, rapid, rhythmic eye movements
- Optic atrophy
- Progressive night blindness
- Retina degeneration
- Visual impairment
- Abnormal central response of multifocal electroretinogram
- Abnormal full-field electroretinogram
- Abnormal optic disc morphology
- Bulging cornea
- Chorioretinal atrophy
- Close sighted
- Cystoid macular edema
- Esodeviation
- Eye muscle paralysis
- Falciform retinal fold
- Glaucoma
- Horizontal nystagmus
- Loss of peripheral vision
- Optic disc drusen
- Peripapillary atrophy
- Photoreceptor outer segment loss on macular OCT
- Retinal atrophy
- Retinal detachment
- Severe near sightedness
- Subretinal fluid
- Tractional retinal detachment
- Abnormal color vision
- Abnormally small eyeball
- Clouding of the lens of the eye
- Cortical cataract
- Epiretinal membrane
- Eye floaters
- Macular edema
- Marked vision impairment
- Patchy atrophy of the retinal pigment epithelium
- Photopsia
- Posterior vitreous detachment
- Retinal exudate
- Retinal hole
- Rhegmatogenous retinal detachment
- Yellowish cloudy center of lens
- Progressive loss of vision
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.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- 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.). ZNF408 gene: zinc finger protein 408. Retrieved 16 October 2026, from https://dantelabs.com/genes/znf408
Dante Labs. ZNF408 gene: zinc finger protein 408 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/znf408
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