Predicted to enable structural molecule activity. Predicted to be involved in bicellular tight junction assembly and cell adhesion. Predicted to be active in bicellular tight junction and plasma membrane. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 29. Orthologous to human CLDN14 (claudin 14). [provided by Alliance of Genome Resources, Apr 2025]
A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in rat Cldn14 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
PMP-22/EMP/MP20/Claudin family
extracellular loop
protein binding
identical protein binding
Pathways
Biological processes and signaling networks where the Cldn14 gene in rat plays a role, providing insight into its function and relevance in health or disease.
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
Plasma Membrane
cellular membrane
tight junctions
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the rat Cldn14 gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
calcium-independent cell-cell adhesion
macromolecular complex assembly
tight junction assembly
cell adhesion
Cellular Component
Where in the cell the gene product is active
tight junction
endoplasmic reticulum
plasma membrane
Molecular Function
What the gene product does at the molecular level
identical protein binding
protein binding
structural molecule activity
Gene-Specific Assays for Results You Can Trust
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