Gene
FDX2
ferredoxin 2
- HGNC 30546↗(opens in a new tab)
- Ensembl gene ENSG00000267673↗(opens in a new tab)
- NCBI Gene 112812↗(opens in a new tab)
Summary
- Cytogenetic location
- 19p13.2
- Coordinates
- Chromosome 19: 10,310,045–10,316,015 (GRCh38)
- Exons
- 5 exons across 6 kb
- Protein
- 183 amino acids
- Also known as
- MGC19604
- Previous symbols
- FDX1L
- MANE Select transcript
- ENST00000393708.3NM_001397406.1
- 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 FDX2 yet. The test sequences your whole genome, so your data includes it all the same.
How FDX2 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 1 kb of the gene's 6 kb; 552 of those bases code for the protein.
How a genome test reads FDX2
4
positions in FDX2 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 6 kb of FDX2, introns included, not only the 1 kb of exons.
Traits linked to FDX2
The Human Phenotype Ontology lists these as features of the rare conditions FDX2 can cause. Each trait's page lists the other genes linked to it.
Abnormality of the musculoskeletal system
- Gowers sign
- Muscle spasm
- Proximal neurogenic muscle weakness
- Breakdown of skeletal muscle
- Involuntary muscle stiffness, contraction, or spasm
- Generalized decreased muscle tone
- Low muscle tone
- Mitochondrial myopathy
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.). FDX2 gene: ferredoxin 2. Retrieved 17 October 2026, from https://dantelabs.com/genes/fdx2
Dante Labs. FDX2 gene: ferredoxin 2 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/fdx2
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