CLDN15 Gene - Claudin 15

Tight junction protein involved in paracellular ion transport and gastrointestinal function

Gene Information Card

Symbol CLDN15
Full Name Claudin 15
Gene Type Protein coding
Chromosomal Location 7q22.1
NCBI Gene ID 24146 ncbi.nlm.nih.gov/gene/24146
Ensembl ID ENSG00000106462
UniProt ID P56746
OMIM ID 615792
HGNC ID 2059
Aliases CLDN15, claudin-15

Description

CLDN15 (Claudin 15) is a protein-coding gene that belongs to the claudin family of tight junction proteins. Claudins are integral membrane proteins that form the backbone of tight junction strands, regulating paracellular ion permeability. CLDN15 is specifically involved in the selective permeability of cations, particularly sodium and potassium, in epithelial tissues. It plays a critical role in gastrointestinal tract function, including intestinal ion absorption and barrier maintenance. The gene is located on chromosome 7q22.1 and encodes a 228-amino acid protein with four transmembrane domains.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Inflammatory Bowel Disease (IBD) Altered tight junction integrity and paracellular permeability due to CLDN15 dysregulation NCBI Gene, PubMed
Colorectal Cancer Downregulation of CLDN15 expression associated with tumor progression and metastasis COSMIC, PubMed
Gastric Cancer Reduced CLDN15 expression linked to poor prognosis and increased invasion COSMIC, PubMed

Expression Profile

Tissue Expression
Tissue nTPM level
Small intestine 45.2 High
Colon 38.1 High
Stomach 12.5 Medium
Kidney 8.3 Medium
Liver 2.1 Low
Cell Line Expression
Cell Line nTPM Notes
Caco-2 52.0 Colorectal adenocarcinoma, high expression
HT-29 41.3 Colorectal adenocarcinoma, moderate expression
HCT 116 35.7 Colorectal carcinoma, moderate expression
MCF7 1.2 Breast cancer, low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.200C>T (p.Pro67Leu) Missense <0.01% Potential alteration in tight junction assembly
c.340G>A (p.Val114Met) Missense <0.01% Unknown functional impact
c.456_457insA Frameshift <0.01% Predicted loss of function
Mutation functional classification

Loss of Function (LOF)

Frameshift mutations (e.g., c.456_457insA) are predicted to cause loss of function by truncating the protein, disrupting tight junction integrity.

Gain of Function (GOF)

No gain-of-function mutations have been reported for CLDN15.

Dominant Negative (DN)

No dominant-negative mutations have been characterized for CLDN15.

Pathways

Tight junction pathway (KEGG: hsa04530)
Cell junction organization (Reactome: R-HSA-446728)

Protein Summary

Claudin-15 is a 228-amino acid transmembrane protein with four membrane-spanning domains, two extracellular loops, and intracellular N- and C-termini. It localizes to tight junctions in epithelial cells, where it forms paracellular pores selective for cations, particularly Na+ and K+. The protein is essential for maintaining ion homeostasis in the gastrointestinal tract, especially in the small intestine and colon. Dysregulation of claudin-15 expression is associated with inflammatory bowel disease and colorectal cancer.

Related Products

Product name Cat.No. Species Gene ID
CLDN15 Knockout HEK293 Cell Line EDJ-KQ7473 Human 24146 Details Get a Quote
CLDN15 Knockout A-549 Cell Line EDJ-KQ34035 Human 24146 Details Get a Quote
CLDN15 Knockout HCT 116 Cell Line EDJ-KQ34037 Human 24146 Details Get a Quote
CLDN15 Knockout HeLa Cell Line EDJ-KQ34038 Human 24146 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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