Scfd2 Gene Summary [Mouse]

Predicted to be involved in intracellular protein transport and vesicle-mediated transport. Orthologous to human SCFD2 (sec1 family domain containing 2). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Protein Coding
Official Symbol
Scfd2
Official Name
Sec1 family domain containing 2 [Source:MGI Symbol;Acc:MGI:2443446]
Ensembl ID
ENSMUSG00000062110
Bio databases IDs NCBI: 212986 Ensembl: ENSMUSG00000062110
Aliases Sec1 family domain containing 2
Synonyms E430013M20RIK, Sec1 family domain containing 2, STXBP1L1
Species
Mouse, Mus musculus
OrthologiesHumanRat

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 mouse Scfd2 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • transporter

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • uterine leiomyoma
  • leiomyomatosis
  • insomnia
  • Alzheimer disease
  • COVID-19
  • open-angle glaucoma
  • covid-19 death
  • male pattern hair loss
  • cataract
  • breast carcinoma

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 Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse Scfd2 gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • vesicle-mediated transport
  • intracellular protein transport

Gene-Specific Assays for Results You Can Trust

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