FCN1 Back

ficolin (collagen/fibrinogen domain containing) 1

External References:      Wikipedia GeneCards HUGO COSMIC Google Scholar

NCBI Description of FCN1

The ficolin family of proteins are characterized by the presence of a leader peptide, a short N-terminal segment, followed by a collagen-like region, and a C-terminal fibrinogen-like domain. The collagen-like and the fibrinogen-like domains are also found separately in other proteins such as complement protein C1q, C-type lectins known as collectins, and tenascins. However, all these proteins recognize different targets, and are functionally distinct. Ficolin 1 encoded by FCN1 is predominantly expressed in the peripheral blood leukocytes, and has been postulated to function as a plasma protein with elastin-binding activity.

Community Annotation of FCN1 Add / Edit FCN1: Annotations

No community annotations yet for FCN1.
Sort mutations by: Tumor type  Mutation type  Position  
Straightedge cursor Expand

Figure notes

• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


FCN1 is highly significantly mutated in
FCN1 is significantly mutated in
FCN1 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for FCN1