Gene
KRT10
keratin 10
- HGNC 6413↗(opens in a new tab)
- Ensembl gene ENSG00000186395↗(opens in a new tab)
- NCBI Gene 3858↗(opens in a new tab)
Summary
- Cytogenetic location
- 17q21.2
- Coordinates
- Chromosome 17: 40,818,117–40,822,614 (GRCh38)
- Exons
- 8 exons across 4.5 kb
- Protein
- 584 amino acids
- Inheritance
- Autosomal dominant
- Also known as
- K10, CK10
- Previous symbols
- KPP
- MANE Select transcript
- ENST00000269576.6NM_000421.5
- 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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Inherited Ichthyoses
- Congenital reticular ichthyosiform erythrodermaAutosomal dominant
A keratin disorder in which red, scaly skin at birth is later dotted with expanding islands of normal skin.
- 1 GenCC submitter rates it definitive or strong
- Epidermolytic ichthyosisAutosomal dominant
A keratin disorder (KRT1/KRT10) with blistering at birth followed by thickened, ridged scaling.
- 5 GenCC submitters rate it definitive or strong
What knowing changes
Diagnosis guides skin care and infection prevention, and informs family planning.
Inheritance
- Autosomal dominant
- One changed copy, from either parent, is enough. A parent who has one passes it on to each child with a one-in-two chance.
How KRT10 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
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 4.5 kb; 1,755 of those bases code for the protein.
How a genome test reads KRT10
9
positions in KRT10 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 4.5 kb of KRT10, introns included, not only the 2.1 kb of exons.
Genes linked to the same conditions
Traits linked to KRT10
The Human Phenotype Ontology lists these as features of the rare conditions KRT10 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.). KRT10 gene: keratin 10. Retrieved 16 October 2026, from https://dantelabs.com/genes/krt10
Dante Labs. KRT10 gene: keratin 10 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/krt10
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