Skip to content
GenoLensGenoLens

KRT3

Chr 12q13.13

keratin 3

Aliases:
CK3, K3
MANE:
ENST00000417996.2

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Corneal abnormalities

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Corneal dystrophy

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
  • Structural eye disease

    MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

Disease associations (Open Targets)

  • corneal dystrophy, Meesmann, 2

    0.67
  • Meesmann corneal dystrophy

    0.60
  • corneal dystrophy

    0.34
  • corneal disorder

    0.28
  • congenital hereditary endothelial dystrophy of cornea

    0.11
  • Sjogren syndrome

    0.08
  • hepatocellular carcinoma

    0.06
  • esophageal adenocarcinoma

    0.04
  • central nervous system cancer

    0.03
  • keratoconus

    0.03

Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.

Protein function (UniProt)

Keratin, type II cytoskeletal 3

Structural component of intermediate filaments in the corneal epithelium. Forms heteropolymers with the type I keratin KRT12, assembling into keratin intermediate filament networks that provide mechanical strength and structural integrity to the corneal epithelial layer

Data sources: HGNC (CC BY 4.0), AlphaFold (CC BY 4.0, Jumper et al. Nature 2021), Genomics England PanelApp (CC BY 4.0), ClinGen, Open Targets (CC0), UniProt.

Not for sole clinical decision-making. Always verify against primary sources.