2. Gene
  3. Fscn2 - fascin actin-bundling protein 2 Gene

Fscn2 - fascin actin-bundling protein 2 Gene

  • Gene
  • Protein
  • Agent
  • Ortholog
Mus musculus

Also known as Ahl8; A930022G03; C630046B20Rik

Gene ID: 238021 | Gene type: protein coding

About Fscn2

Summary

Predicted to enable actin filament binding activity. Acts upstream of or within eye photoreceptor cell development. Located in actin Cytoskeleton and stereocilium. Is expressed in retina. Used to study auditory system disease; retinal degeneration; and retinitis pigmentosa 30. Human ortholog(s) of this gene implicated in retinitis pigmentosa and retinitis pigmentosa 30. Orthologous to human FSCN2 (fascin actin-bundling protein 2, retinal). [provided by Alliance of Genome Resources, Apr 2022]

Fscn2 Products(1)

mRNA Protein Name
NM_172802.4 NP_766390.2 fascin-2
Protein Preferred Names Protein Names

fascin-2

fascin homolog 2, actin-bundling protein, retinal

retinal fascin

Related Agents

Pre-clinical Phase
Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-RS05120 FSCN2 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Fscn2 NCBI NCBI:25794