KRT15 Gene (Keratin 15)

Intermediate filament protein involved in epithelial integrity and hair follicle biology

Gene Information Card

Symbol KRT15
Full Name Keratin 15
Gene Type Protein coding
Chromosomal Location 17q21.2
NCBI Gene ID 3866 ncbi.nlm.nih.gov/gene/3866
Ensembl ID ENSG00000171346
UniProt ID P19012
OMIM ID 148030
HGNC ID 6422
Aliases K15, CK15, K1CO, cytokeratin 15

Description

KRT15 encodes keratin 15, a type I intermediate filament protein expressed primarily in the basal layer of stratified epithelia and the outer root sheath of hair follicles. It plays a critical role in maintaining epithelial structural integrity and is a marker for epithelial stem cells in the hair follicle bulge. KRT15 is frequently used as a biomarker in cancer studies, particularly in breast and skin cancers.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast Cancer KRT15 overexpression is associated with basal-like subtype and poor prognosis; may promote invasion and metastasis. NCBI Gene, COSMIC
Squamous Cell Carcinoma Loss of KRT15 expression correlates with dedifferentiation and aggressive tumor behavior. ClinVar, COSMIC
Hair Follicle Disorders Mutations in KRT15 can disrupt hair follicle integrity, leading to alopecia or abnormal hair growth. OMIM
Epidermolysis Bullosa Simplex Rare KRT15 mutations may contribute to skin fragility phenotypes. ClinVar

Expression Profile

Tissue Expression
Tissue nTPM level
Skin 45.2 High
Esophagus 38.1 High
Breast 12.5 Medium
Prostate 8.3 Medium
Lung 5.1 Low
Cell Line Expression
Cell Line nTPM Notes
HaCaT (keratinocyte) 62.4 High expression; used as positive control
MCF-7 (breast cancer) 18.7 Moderate expression; basal-like subtype
A549 (lung cancer) 4.2 Low expression
HeLa (cervical cancer) 9.8 Medium expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.315C>T (p.Arg105Cys) Missense <0.1% Alters filament assembly; associated with skin fragility
c.487G>A (p.Gly163Arg) Missense <0.1% Disrupts keratin network; reported in epidermolysis bullosa
c.1A>G (p.Met1Val) Start loss Rare Loss of protein expression; potential loss-of-function
Mutation functional classification

Loss of Function (LOF)

Start loss and nonsense mutations lead to truncated or absent keratin 15, compromising epithelial integrity.

Gain of Function (GOF)

Not well documented; some missense variants may alter filament dynamics but no clear gain-of-function reported.

Dominant Negative (DN)

Missense mutations in the rod domain can disrupt filament assembly in a dominant-negative manner, causing skin fragility.

Pathways

Intermediate filament organization (Reactome: R-HSA-6809371)
Keratinization (Reactome: R-HSA-6805567)
Formation of the cornified envelope (Reactome: R-HSA-6809374)

Protein Summary

Keratin 15 is a 50 kDa type I intermediate filament protein that heteropolymerizes with type II keratins to form cytoskeletal networks. It is predominantly expressed in the basal layer of stratified epithelia and the outer root sheath of hair follicles. KRT15 serves as a marker for epithelial stem cells and is implicated in tissue integrity, wound healing, and cancer progression. Mutations can lead to skin fragility disorders, while altered expression is observed in various carcinomas.

Related Products

Product name Cat.No. Species Gene ID
KRT15 Knockout HEK293 Cell Line EDJ-KQ5093 Human 3866 Details Get a Quote
KRT15 Knockout A-549 Cell Line EDJ-KQ28040 Human 3866 Details Get a Quote
KRT15 Knockout HCT 116 Cell Line EDJ-KQ28041 Human 3866 Details Get a Quote
KRT15 Knockout HeLa Cell Line EDJ-KQ28042 Human 3866 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
Contact Us
*
*
*
*
How did you hear about us: