Gene
KRT12
keratin 12
- HGNC 6414↗(opens in a new tab)
- Ensembl gene ENSG00000187242↗(opens in a new tab)
- NCBI Gene 3859↗(opens in a new tab)
Summary
- Cytogenetic location
- 17q21.2
- Coordinates
- Chromosome 17: 40,861,303–40,867,223 (GRCh38)
- Exons
- 8 exons across 5.9 kb
- Protein
- 494 amino acids
- Also known as
- K12
- MANE Select transcript
- ENST00000251643.5NM_000223.4
- 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.
Read KRT12, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome TestCurated report relevant to this gene
Hereditary Corneal Dystrophies
- Corneal Dystrophy
A group of inherited conditions affecting one or more layers of the cornea, including Fuchs endothelial dystrophy (often linked to a TCF4 repeat expansion), TGFBI-related granular and lattice dystrophies, and rarer types caused by genes such as SLC4A11, COL8A2, ZEB1 and CHST6.
- 3 GenCC submitters rate it definitive or strong
What knowing changes
Carriers of TGFBI variants are generally advised to avoid laser refractive surgery (LASIK or PRK), which can make deposits worse; corneal transplant can restore vision in advanced disease.
How KRT12 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
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 5.9 kb; 1,485 of those bases code for the protein.
Genes linked to the same conditions
- CHST6carbohydrate sulfotransferase 6Shares 1 condition
- COL17A1collagen type XVII alpha 1 chainShares 1 condition
- COL8A2collagen type VIII alpha 2 chainShares 1 condition
- DCNdecorinShares 1 condition
- GRHL2grainyhead like transcription factor 2Shares 1 condition
- GSNgelsolinShares 1 condition
- KRT3keratin 3Shares 1 condition
- MCOLN1mucolipin TRP cation channel 1Shares 1 condition
- NLRP1NLR family pyrin domain containing 1Shares 1 condition
- OVOL2ovo like zinc finger 2Shares 1 condition
- PIKFYVEphosphoinositide kinase, FYVE-type zinc finger containingShares 1 condition
- PRDX3peroxiredoxin 3Shares 1 condition
Traits linked to KRT12
The Human Phenotype Ontology lists these as features of the rare conditions KRT12 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.
- 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.). KRT12 gene: keratin 12. Retrieved 16 October 2026, from https://dantelabs.com/genes/krt12
Dante Labs. KRT12 gene: keratin 12 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/krt12
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks