KRT19 (Keratin 19)

Type I Cytoskeletal Keratin, Intermediate Filament Protein

Gene Information Card

Symbol KRT19
Full Name Keratin 19
Gene Type Protein coding
Chromosomal Location 17q21.2
NCBI Gene ID 3880 ncbi.nlm.nih.gov/gene/3880
Ensembl ID ENSG00000171345
UniProt ID P08727
OMIM ID 148020
HGNC ID 6429
Aliases CK19, K19, K1CS, MGC15366

Description

KRT19 (Keratin 19) encodes a type I cytokeratin, a member of the intermediate filament family. Keratin 19 is expressed in simple epithelia, including intestinal, pancreatic, biliary, and mammary epithelium. It is a key marker for circulating tumor cells (CTCs) and is frequently used in immunohistochemistry to detect epithelial-derived carcinomas. KRT19 expression is regulated during development and is often upregulated in cancers such as cholangiocarcinoma, pancreatic ductal adenocarcinoma, and breast cancer.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cholangiocarcinoma Overexpression of KRT19 in bile duct epithelium promotes tumor cell invasion and metastasis. PMID: 25695633
Pancreatic Ductal Adenocarcinoma KRT19 is a marker of aggressive tumor phenotype and correlates with poor prognosis. PMID: 25964277
Breast Cancer KRT19-positive circulating tumor cells are associated with metastatic relapse and reduced survival. PMID: 22962440
Hepatocellular Carcinoma KRT19 expression in hepatic progenitor cells indicates a more aggressive subtype. PMID: 19177562

Expression Profile

Tissue Expression
Tissue nTPM level
Pancreas 68.5 High
Gallbladder 55.2 High
Breast 42.1 High
Liver 12.3 Medium
Colon 8.7 Low
Cell Line Expression
Cell Line nTPM Notes
MCF7 (Breast cancer) 45.2 High expression; used as positive control for KRT19
PANC-1 (Pancreatic cancer) 62.8 High expression; correlates with invasive phenotype
HepG2 (Hepatocellular carcinoma) 15.4 Moderate expression
A549 (Lung cancer) 3.1 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1A>G (p.Met1?) Missense Rare Likely loss of function; reported in ClinVar
c.315G>A (p.Trp105*) Nonsense <0.01% Premature stop; loss of function
c.428C>T (p.Pro143Leu) Missense <0.01% Uncertain significance; no functional data
Mutation functional classification

Loss of Function (LOF)

Nonsense and frameshift mutations in KRT19 are rare and predicted to cause haploinsufficiency, but no clear disease phenotype has been established.

Gain of Function (GOF)

No gain-of-function mutations have been reported for KRT19.

Dominant Negative (DN)

No dominant-negative mutations have been characterized for KRT19.

Pathways

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

Protein Summary

Keratin 19 (KRT19) is a 40 kDa type I intermediate filament protein that forms heteropolymers with type II keratins (e.g., KRT8, KRT18). It is expressed in simple epithelia and is a major component of the cytoskeleton. KRT19 is widely used as a biomarker for epithelial-derived tumors and circulating tumor cells. Its expression is regulated by transcription factors such as GATA6 and HNF1A. Post-translational modifications include phosphorylation, which modulates filament dynamics.

Related Products

Product name Cat.No. Species Gene ID
KRT19 Knockout HEK293 Cell Line EDJ-KQ3214 Human 3880 Details Get a Quote
KRT19 Knockout A-549 Cell Line EDJ-KQ24691 Human 3880 Details Get a Quote
KRT19 Knockout HCT 116 Cell Line EDJ-KQ24692 Human 3880 Details Get a Quote
KRT19 Knockout HeLa Cell Line EDJ-KQ24693 Human 3880 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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