FCN2 - ficolin 2 Gene
Also Known as P35; FCNL; EBP-37; ficolin-2
Species: Homo sapiens
About FCN2
This gene has 2 transcripts (splice variants), 20 orthologues and 25 paralogues. Biased expression in liver (RPKM 10.3), adrenal (RPKM 1.6) and 2 other tissues.
Summary
The product of this gene belongs to the ficolin family of proteins. This family is 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. This gene is predominantly expressed in the liver, and has been shown to have carbohydrate binding and opsonic activities. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
FCN2 Products (2)
| mRNA | Protein | Name |
|---|---|---|
| NM_004108.3 | NP_004099.2 | ficolin-2 isoform a precursor |
| NM_015837.3 | NP_056652.1 | ficolin-2 isoform b precursor |
FCN2 Protein Structure
Collagen: Collagen triple helix repeat (20 copies) (50 - 95)
Fibrinogen_C: Fibrinogen beta and gamma chains, C-terminal globular domain (102 - 312)
- 0
- 100
- 200
- 313 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
ficolin-2 |
|
FCN2 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
FCN2 | Q15485 | FCN3 | Homo sapiens | O75636 | 32094208 | |
|
Intra
|
FCN2 | Q15485 | FCN3 | Homo sapiens | O75636 | 32094208 | |
|
Intra
|
FCN2 | Q15485 | FCN3 | Homo sapiens | O75636 | 32094208 | |
|
Intra
|
FCN2 | Q15485 | FCN3 | Homo sapiens | O75636 | 23785123 |
FCN2 Antibodies
| Cat. No. | Product Name | Application | Reactivity |
|---|---|---|---|
| HY-P89948 | L-ficolin Antibody (YA9292) | WB, ELISA | human |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Rheumatic Fever |
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| Rheumatic Heart Disease |
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| Chagas Disease |
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| Schistosomiasis |
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| Adenoiditis |
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| 3mc Syndrome |
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| 3mc Syndrome 2 |
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| Dermatitis, Atopic, 3 |
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| Common Variable Immunodeficiency |
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| Borderline Leprosy |
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| Invasive Aspergillosis |
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| Leprosy 3 |
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| Hemolytic Uremic Syndrome, Atypical 1 |
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| Malaria |
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