Gene
KY
kyphoscoliosis peptidase
- HGNC 26576↗(opens in a new tab)
- Ensembl gene ENSG00000174611↗(opens in a new tab)
- NCBI Gene 339855↗(opens in a new tab)
Summary
- Cytogenetic location
- 3q22.2
- Coordinates
- Chromosome 3: 134,599,923–134,651,022 (GRCh38)
- Exons
- 11 exons across 51.1 kb
- Protein
- 661 amino acids
- Also known as
- FLJ33207
- MANE Select transcript
- ENST00000423778.7NM_178554.6
- 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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Myofibrillar Myopathies
- Myofibrillar myopathy
A group of muscle disorders in which the contractile structure of muscle fibers breaks down, caused by genes such as DES, CRYAB, MYOT, LDB3, FLNC and BAG3.
- 2 GenCC submitters rate it definitive or strong
What knowing changes
Because the heart is often involved, regular heart checks (such as ECG and echocardiography) are recommended even without symptoms.
How KY 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 5.7 kb of the gene's 51.1 kb; 1,986 of those bases code for the protein.
How a genome test reads KY
5
positions in KY 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 51.1 kb of KY, introns included, not only the 5.7 kb of exons.
Genes linked to the same conditions
- BAG3BAG cochaperone 3Shares 1 condition
- CRYABcrystallin alpha BShares 1 condition
- DESdesminShares 1 condition
- FLNCfilamin CShares 1 condition
- HSPB8heat shock protein family B (small) member 8Shares 1 condition
- LDB3LIM domain binding 3Shares 1 condition
- MYOTmyotilinShares 1 condition
- PYROXD1pyridine nucleotide-disulphide oxidoreductase domain 1Shares 1 condition
- RYR1ryanodine receptor 1Shares 1 condition
- SVILsupervillinShares 1 condition
- TTNtitinShares 1 condition
- UNC45Bunc-45 myosin chaperone BShares 1 condition
Traits linked to KY
The Human Phenotype Ontology lists these as features of the rare conditions KY can cause. Each trait's page lists the other genes linked to it.
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.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- 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.). KY gene: kyphoscoliosis peptidase. Retrieved 16 October 2026, from https://dantelabs.com/genes/ky
Dante Labs. KY gene: kyphoscoliosis peptidase [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/ky
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