Elmod3

Predicted to act upstream of or within several processes, including cilium assembly; inner ear receptor cell development; and sensory perception of sound. Predicted to be located in cytoskeleton; kinocilium; and stereocilium. Predicted to be active in Golgi apparatus and cilium. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 81 and autosomal recessive nonsyndromic deafness 88. Orthologous to human ELMOD3 (ELMO domain containing 3). [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 Elmod3 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 rat Elmod3 gene, providing context for its role in the cell.