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Gene

CWC27

CWC27 spliceosome associated cyclophilin

Summary

Cytogenetic location
5q12.3
Coordinates
Chromosome 5: 64,768,930–65,018,750 (GRCh38)
Exons
14 exons across 249.8 kb
Protein
472 amino acids
Also known as
NY-CO-10, SDCCAG-10
Previous symbols
SDCCAG10
MANE Select transcript
ENST00000381070.8NM_005869.4
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 CWC27 yet. The test sequences your whole genome, so your data includes it all the same.

How CWC27 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 5, with a bracket where CWC27 sits. CWC27 and 4 genes near it on chromosome 5, from 64,393,840 to 65,393,839.Chromosome 55q12.3p15.33p15.32p15.31p15.2p15.1p14.3p14.2p14.1p13.3p13.2p13.1p12p11q11.1q11.2q12.1q12.2q12.3q13.1q13.2q13.3q14.1q14.2q14.3q15q21.1q21.2q21.3q22.1q22.2q22.3q23.1q23.2q23.3q31.1q31.2q31.3q32q33.1q33.2q33.3q34q35.1q35.2q35.364.4 Mb64.6 Mb64.8 Mb65 Mb65.2 MbRGS7BP: 64,505,934–64,614,661, forward strandRGS7BPSHISAL2B: 64,690,194–64,718,192, forward strandSHISAL2BSREK1IP1: 64,718,148–64,768,702, reverse strandSREK1IP1CWC27: 64,768,930–65,018,750, forward strandCWC27ADAMTS6: 65,148,738–65,481,944, reverse strandADAMTS6Diagram of CWC27: 14 exons on the forward strand of chromosome 5Exon 3: 1 known disease-causing siteExon 4: 1 known disease-causing siteExon 5: 1 known disease-causing siteExon 7: 1 known disease-causing siteExon 9: 1 known disease-causing siteExon 10: 2 known disease-causing sitesExon 11: 1 known disease-causing siteExon 12: 1 known disease-causing siteExon 1: 64,768,930–64,769,188, 259 basesExon 2: 64,774,691–64,774,787, 97 basesExon 3: 64,781,921–64,782,033, 113 basesExon 4: 64,783,836–64,783,979, 144 basesExon 5: 64,785,481–64,785,579, 99 basesExon 6: 64,786,524–64,786,627, 104 basesExon 7: 64,788,951–64,789,020, 70 basesExon 8: 64,800,248–64,800,327, 80 basesExon 9: 64,801,302–64,801,332, 31 basesExon 10: 64,804,229–64,804,386, 158 basesExon 11: 64,885,443–64,885,546, 104 basesExon 12: 64,971,703–64,971,812, 110 basesExon 13: 64,977,135–64,977,238, 104 basesExon 14: 65,018,159–65,018,750, 592 bases1510145′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 2.1 kb of the gene's 249.8 kb; 1,419 of those bases code for the protein.

How a genome test reads CWC27

14

positions in CWC27 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 249.8 kb of CWC27, introns included, not only the 2.1 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.). CWC27 gene: CWC27 spliceosome associated cyclophilin. Retrieved 16 October 2026, from https://dantelabs.com/genes/cwc27

Vancouver

Dante Labs. CWC27 gene: CWC27 spliceosome associated cyclophilin [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/cwc27

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