SPRR2D Gene Summary [Human]

Predicted to be involved in keratinization. Predicted to act upstream of or within female gonad development and response to estradiol. Located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

Details

Type
Protein Coding
Official Symbol
SPRR2D
Official Name
small proline rich protein 2D [Source:HGNC Symbol;Acc:HGNC:11264]
Ensembl ID
ENSG00000163216
Bio databases IDs NCBI: 6703 Ensembl: ENSG00000163216
Aliases small proline rich protein 2D
Synonyms small proline rich protein 2D, SPR-2D
Species
Human, Homo sapiens

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • chronic periodontal disease
  • plaque psoriasis
regulated by

Subcellular Expression

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

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human SPRR2D gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • epidermis development
  • keratinization

Cellular Component

Where in the cell the gene product is active
  • cornified envelope
  • cytoplasm
  • cytosol

Gene-Specific Assays for Results You Can Trust

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