SPRYD3 Gene Summary [Human]

Predicted to be involved in cell surface receptor signaling pathway and cytoskeleton organization. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

Details

Type
Protein Coding
Official Symbol
SPRYD3
Official Name
SPRY domain containing 3 [Source:HGNC Symbol;Acc:HGNC:25920]
Ensembl ID
ENSG00000167778
Bio databases IDs NCBI: 84926 Ensembl: ENSG00000167778
Aliases SPRY domain containing 3
Synonyms RGD1561500, SPRY domain containing 3
Species
Human, Homo sapiens
OrthologiesMouseRat

Protein Domains

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 human SPRYD3 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • SPRY domain

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • insulin-dependent diabetes mellitus
  • pervasive developmental disorder

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Unknown

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.