Sprr1b

Predicted to be a structural constituent of cytoskeleton. Predicted to be involved in cytoskeleton organization and keratinization. Predicted to act upstream of or within regulation of cell shape. Predicted to be located in Golgi apparatus; cornified envelope; and perinuclear region of cytoplasm. Is expressed in several structures, including alimentary system; genitourinary system; nervous system; skin; and thymus. Orthologous to human SPRR1B (small proline rich protein 1B). [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 mouse Sprr1b often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.

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.

Describes the biological processes, cellular components, and molecular functions associated with the mouse Sprr1b gene, providing context for its role in the cell.