Gene
ZNF699
zinc finger protein 699
- HGNC 24750↗(opens in a new tab)
- Ensembl gene ENSG00000196110↗(opens in a new tab)
- NCBI Gene 374879↗(opens in a new tab)
Summary
- Cytogenetic location
- 19p13.2
- Coordinates
- Chromosome 19: 9,291,140–9,309,838 (GRCh38)
- Exons
- 6 exons across 18.7 kb
- Protein
- 642 amino acids
- Also known as
- FLJ38144
- MANE Select transcript
- ENST00000591998.6NM_198535.3
- 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 ZNF699 yet. The test sequences your whole genome, so your data includes it all the same.
How ZNF699 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 6.8 kb of the gene's 18.7 kb; 1,929 of those bases code for the protein.
How a genome test reads ZNF699
9
positions in ZNF699 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 18.7 kb of ZNF699, introns included, not only the 6.8 kb of exons.
Traits linked to ZNF699
The Human Phenotype Ontology lists these as features of the rare conditions ZNF699 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the digestive system
- Intestinal atresia
- Jejunal atresia
- Acid reflux
- Enlarged liver
- Feeding difficulties
- Nasogastric tube feeding
- Oral-pharyngeal dysphagia
- Poor suck
Show 3 more traits
Abnormality of the genitourinary system
- Abnormal renal cortex morphology
- Abnormal renal medulla morphology
- Ambiguous external genitalia
- Bilateral renal dysplasia
- Bilateral renal hypoplasia
- Chordee
- Chronic kidney disease
- Frequent urinary tract infections
Show 3 more traits
Abnormality of limbs
- Webbed fingers or toes
- Asymmetric overgrowth
- Club feet
- Extra thumb
- Fused toes
- Hemihypotrophy of lower limb
- Knock knees
- More than five fingers or toes on hands or feet
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.). ZNF699 gene: zinc finger protein 699. Retrieved 17 October 2026, from https://dantelabs.com/genes/znf699
Dante Labs. ZNF699 gene: zinc finger protein 699 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/znf699
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