VNN3 Gene Summary [Human]

This gene is the central gene in a cluster of three vanin genes on chromosome 6q23-q24. Extensive alternative splicing has been described; the two most common variants are represented as RefSeqs. [provided by RefSeq, Apr 2014]

Details

Type
Protein Coding
Official Symbol
VNN3
Official Name
vanin 3 [Source:HGNC Symbol;Acc:HGNC:16431]
Ensembl ID
ENSG00000093134
Bio databases IDs NCBI: 55350 Ensembl: ENSG00000093134
Aliases vanin 3, vanin 3, pseudogene
Synonyms HSA238982, vanin 3, pseudogene, VNN3
Species
Human, Homo sapiens

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 VNN3 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • enzyme

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
binds
disease
  • psoriasis
regulated by
  • lipopolysaccharide
  • HIV-1 BaL

Subcellular Expression

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

Gene-Specific Assays for Results You Can Trust

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