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Gene

FTCD

formimidoyltransferase cyclodeaminase

Summary

Cytogenetic location
21q22.3
Coordinates
Chromosome 21: 46,136,779–46,155,579 (GRCh38)
Exons
14 exons across 18.8 kb
Protein
541 amino acids
MANE Select transcript
ENST00000397746.8NM_206965.2
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 FTCD yet. The test sequences your whole genome, so your data includes it all the same.

How FTCD is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 21, with a bracket where FTCD sits. FTCD and 13 genes near it on chromosome 21, from 45,646,179 to 46,646,178.Chromosome 2121q22.3p13p12p11.2p11.1q11.1q11.2q21.1q21.2q21.3q22.11q22.12q22.13q22.2q22.345.8 Mb46 Mb46.2 Mb46.4 Mb46.6 MbPCBP3: 45,643,661–45,942,454, forward strandPCBP3COL6A1: 45,981,727–46,005,050, forward strandCOL6A1COL6A2: 46,096,722–46,132,851, forward strandCOL6A2FTCD: 46,136,779–46,155,579, reverse strandFTCDSPATC1L: 46,161,148–46,184,476, reverse strandSPATC1LLSS: 46,187,299–46,228,840, reverse strandLSSMCM3AP: 46,232,689–46,286,617, reverse strandMCM3APYBEY: 46,285,831–46,313,301, forward strandYBEYC21orf58: 46,291,929–46,324,470, reverse strandC21orf58PCNT: 46,324,082–46,445,769, forward strandPCNT: 46,326,288–46,326,491, forward strandDIP2A: 46,458,841–46,572,746, forward strandDIP2AS100B: 46,598,355–46,605,208, reverse strandS100BPRMT2: 46,635,197–46,666,229, forward strandPRMT2Diagram of FTCD: 14 exons on the reverse strand of chromosome 21Exon 14: 2 known disease-causing sitesExon 13: 1 known disease-causing siteExon 12: 1 known disease-causing siteExon 11: 2 known disease-causing sitesExon 9: 11 known disease-causing sitesExon 8: 1 known disease-causing siteExon 6: 2 known disease-causing sitesExon 5: 3 known disease-causing sitesExon 4: 2 known disease-causing sitesExon 3: 4 known disease-causing sitesExon 2: 2 known disease-causing sitesExon 14: 46,136,779–46,137,073, 295 basesExon 13: 46,137,239–46,137,334, 96 basesExon 12: 46,138,508–46,138,646, 139 basesExon 11: 46,138,880–46,138,923, 44 basesExon 10: 46,145,417–46,145,578, 162 basesExon 9: 46,145,818–46,145,947, 130 basesExon 8: 46,146,266–46,146,327, 62 basesExon 7: 46,150,119–46,150,250, 132 basesExon 6: 46,150,388–46,150,525, 138 basesExon 5: 46,151,558–46,151,737, 180 basesExon 4: 46,151,892–46,151,980, 89 basesExon 3: 46,152,907–46,153,035, 129 basesExon 2: 46,154,149–46,154,332, 184 basesExon 1: 46,155,470–46,155,579, 110 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 1.9 kb of the gene's 18.8 kb; 1,626 of those bases code for the protein.

How a genome test reads FTCD

38

positions in FTCD 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 18.8 kb of FTCD, introns included, not only the 1.9 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.). FTCD gene: formimidoyltransferase cyclodeaminase. Retrieved 16 October 2026, from https://dantelabs.com/genes/ftcd

Vancouver

Dante Labs. FTCD gene: formimidoyltransferase cyclodeaminase [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/ftcd

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