Puneet Varma (Editor)

INF2

Updated on
Edit
Like
Comment
Share on FacebookTweet on TwitterShare on LinkedInShare on Reddit
Species
  
Human

Entrez
  
64423

Human
  
Mouse

Ensembl
  
ENSG00000203485

INF2

Aliases
  
INF2, C14orf151, C14orf173, CMTDIE, FSGS5, pp9484, inverted formin, FH2 and WH2 domain containing

External IDs
  
MGI: 1917685 HomoloGene: 82406 GeneCards: INF2

Inverted formin-2 is a protein that in humans is encoded by the INF2 gene. It belongs to the protein family called the formins. It has two splice isoforms, CAAX which localizes to the endoplasmic reticulum and non-CAAX which localizes to focal adhesions and the cytoplasm with enrichment at the Golgi. INF2 plays a role in mitochondrial fission and dorsal stress fiber formation. INF2 accelerates actin nucleation and elongation by interacting with barbed ends (fast-growing ends) of actin filaments, but also accelerates depolymerization of actin through encircling and severing filaments.

Clinical significance

It can be associated with Focal segmental glomerulosclerosis and Charcot-Marie Tooth Disease.

References

INF2 Wikipedia