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Gene

FRA10AC1

FRA10A associated CGG repeat 1

Summary

Cytogenetic location
10q23.33
Coordinates
Chromosome 10: 93,667,883–93,702,592 (GRCh38)
Exons
14 exons across 34.7 kb
Protein
315 amino acids
Previous symbols
C10orf4
MANE Select transcript
ENST00000359204.5NM_145246.5
Locus type
gene with protein product
  • Very high
  • Confident
  • Low
  • Very low

Reference genomeGRCh38

Positions on gene and variant pages follow this choice, in this browser.

Curated reports relevant to this gene

No Genome Test report reads FRA10AC1 yet. The test sequences your whole genome, so your data includes it all the same.

How FRA10AC1 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 10, with a bracket where FRA10AC1 sits. FRA10AC1 and 8 genes near it on chromosome 10, from 93,185,238 to 94,185,237.Chromosome 1010q23.33p15.3p15.2p15.1p14p13p12.33p12.32p12.31p12.2p12.1p11.23p11.22p11.21p11.1q11.1q11.21q11.22q11.23q21.1q21.2q21.3q22.1q22.2q22.3q23.1q23.2q23.31q23.32q23.33q24.1q24.2q24.31q24.32q24.33q25.1q25.2q25.3q26.11q26.12q26.13q26.2q26.393.2 Mb93.4 Mb93.6 Mb93.8 Mb94 MbMYOF: 93,306,429–93,482,334, reverse strandMYOFCEP55: 93,496,577–93,529,096, forward strandCEP55FFAR4: 93,566,653–93,605,840, forward strandFFAR4RBP4: 93,590,170–93,603,110, reverse strandRBP4PDE6C: 93,612,533–93,666,010, forward strandPDE6CFRA10AC1: 93,667,883–93,702,592, reverse strandFRA10AC1LGI1: 93,757,840–93,806,272, forward strandLGI1SLC35G1: 93,893,918–93,956,062, forward strandSLC35G1PLCE1: 93,993,807–94,332,823, forward strandPLCE1Diagram of FRA10AC1: 14 exons on the reverse strand of chromosome 10Exon 8: 2 known disease-causing sitesExon 7: 1 known disease-causing siteExon 6: 1 known disease-causing siteExon 2: 2 known disease-causing sitesExon 14: 93,667,883–93,669,868, 1,986 basesExon 13: 93,670,770–93,670,848, 79 basesExon 12: 93,676,653–93,676,691, 39 basesExon 11: 93,681,480–93,681,598, 119 basesExon 10: 93,684,056–93,684,098, 43 basesExon 9: 93,685,246–93,685,359, 114 basesExon 8: 93,687,404–93,687,449, 46 basesExon 7: 93,692,009–93,692,093, 85 basesExon 6: 93,692,646–93,692,729, 84 basesExon 5: 93,694,861–93,694,937, 77 basesExon 4: 93,698,136–93,698,181, 46 basesExon 3: 93,698,301–93,698,396, 96 basesExon 2: 93,700,030–93,700,106, 77 basesExon 1: 93,702,375–93,702,592, 218 bases141210864215′3′

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 3.1 kb of the gene's 34.7 kb; 948 of those bases code for the protein.

How a genome test reads FRA10AC1

8

positions in FRA10AC1 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 34.7 kb of FRA10AC1, introns included, not only the 3.1 kb of exons.

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

APA

Dante Labs. (n.d.). FRA10AC1 gene: FRA10A associated CGG repeat 1. Retrieved 17 October 2026, from https://dantelabs.com/genes/fra10ac1

Vancouver

Dante Labs. FRA10AC1 gene: FRA10A associated CGG repeat 1 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/fra10ac1

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