Gene
PHF7
PHD finger protein 7
- HGNC 18458↗(opens in a new tab)
- Ensembl gene ENSG00000010318↗(opens in a new tab)
- NCBI Gene 51533↗(opens in a new tab)
Summary
- Cytogenetic location
- 3p21.1
- Coordinates
- Chromosome 3: 52,410,660–52,423,641 (GRCh38)
- Exons
- 11 exons across 13 kb
- Protein
- 381 amino acids
- Also known as
- NYD-SP6, HSPC226
- MANE Select transcript
- ENST00000327906.8NM_016483.7
- 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 PHF7 yet. The test sequences your whole genome, so your data includes it all the same.
How PHF7 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- 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 13 kb; 1,146 of those bases code for the protein.
How a genome test reads PHF7
3
positions in PHF7 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 13 kb of PHF7, introns included, not only the 2.1 kb of exons.
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.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). PHF7 gene: PHD finger protein 7. Retrieved 17 October 2026, from https://dantelabs.com/genes/phf7
Dante Labs. PHF7 gene: PHD finger protein 7 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/phf7
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