Gene
FOXD3
forkhead box D3
- HGNC 3804↗(opens in a new tab)
- Ensembl gene ENSG00000187140↗(opens in a new tab)
- NCBI Gene 27022↗(opens in a new tab)
Summary
- Cytogenetic location
- 1p31.3
- Coordinates
- Chromosome 1: 63,322,567–63,325,128 (GRCh38)
- Exons
- 1 exon across 2.6 kb
- Protein
- 478 amino acids
- Also known as
- Genesis, HFH2
- MANE Select transcript
- ENST00000371116.4NM_012183.3
- 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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How FOXD3 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 2.6 kb of the gene's 2.6 kb; 1,437 of those bases code for the protein.
Traits linked to FOXD3
The Human Phenotype Ontology lists these as features of the rare conditions FOXD3 can cause. Each trait's page lists the other genes linked to it.
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.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
Cite this page
Dante Labs. (n.d.). FOXD3 gene: forkhead box D3. Retrieved 17 October 2026, from https://dantelabs.com/genes/foxd3
Dante Labs. FOXD3 gene: forkhead box D3 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/foxd3
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