Gene
FRG1
FSHD region gene 1
- HGNC 3954↗(opens in a new tab)
- Ensembl gene ENSG00000109536↗(opens in a new tab)
- NCBI Gene 2483↗(opens in a new tab)
Summary
- Cytogenetic location
- 4q35.2
- Coordinates
- Chromosome 4: 189,940,872–189,963,192 (GRCh38)
- Exons
- 9 exons across 22.3 kb
- Protein
- 258 amino acids
- Also known as
- FSG1, FRG1A
- MANE Select transcript
- ENST00000226798.9NM_004477.3
- 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 FRG1 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 1 kb of the gene's 22.3 kb; 777 of those bases code for the protein.
Traits linked to FRG1
The Human Phenotype Ontology lists these as features of the rare conditions FRG1 can cause. Each trait's page lists the other genes linked to it.
Abnormality of head or neck
- Expressionless face
- Decreased facial expression
- Eyelids stay open at night
- Pink eye
- Weakness of facial musculature
- Bell's palsy
- Inability to protrude lips
- Inability to puff cheeks
Show 2 more traits
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.). FRG1 gene: FSHD region gene 1. Retrieved 17 October 2026, from https://dantelabs.com/genes/frg1
Dante Labs. FRG1 gene: FSHD region gene 1 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/frg1
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