Identity
HGNC
LOCATION
1q24.2
LOCUSID
ALIAS
FVL,PCCF,RPRGL1,THPH2
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 2153
MIM: 612309
HGNC: 3542
Ensembl: ENSG00000198734
Variants:
dbSNP: 2153
ClinVar: 2153
TCGA: ENSG00000198734
COSMIC: F5
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000198734 | ENST00000367796 | A0A0A0MRJ7 |
| ENSG00000198734 | ENST00000367797 | P12259 |
Expression (GTEx)
Pathways
PharmGKB
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 37639740 | 2024 | Molecular and clinical characterization of two unrelated families with factor V deficiency, including a novel nonsense variant (p.Gln1532*). | 0 |
| 38112128 | 2024 | Autoimmune-acquired coagulation factor V deficiency with hyperfibrinolytic disseminated intravascular coagulation. | 0 |
| 38225166 | 2024 | Determination of vWF, ADAMTS-13 and Thrombospondin-1 in Venous Thromboembolism and Relating Them to the Presence of Factor V Leiden Mutation. | 0 |
| 37639740 | 2024 | Molecular and clinical characterization of two unrelated families with factor V deficiency, including a novel nonsense variant (p.Gln1532*). | 0 |
| 38112128 | 2024 | Autoimmune-acquired coagulation factor V deficiency with hyperfibrinolytic disseminated intravascular coagulation. | 0 |
| 38225166 | 2024 | Determination of vWF, ADAMTS-13 and Thrombospondin-1 in Venous Thromboembolism and Relating Them to the Presence of Factor V Leiden Mutation. | 0 |
| 33993312 | 2023 | Stroke in Young Military Men With Heterozygous for MTHFR Gene Mutation or Factor V Leiden Gene Mutation Associated With Patent Foramen Ovale: Report of Two Cases and Therapeutic Strategy. | 1 |
| 35946468 | 2023 | Congenital factor V deficiency in Taiwan: identification of a novel variant p.Tyr1813 ∗ and two variants specific to East Asians. | 0 |
| 36165080 | 2023 | Patients with severe coronavirus disease 2019 have high frequency of factor 5 Leiden and prothrombin gene mutations. | 1 |
| 36780344 | 2023 | Impaired factor V-related anticoagulant mechanisms and deep vein thrombosis associated with A2086D and W1920R mutations. | 2 |
| 36946317 | 2023 | IL16 and factor V gene variations are associated with asparaginase-related thrombosis in childhood acute lymphoblastic leukemia patients. | 0 |
| 37053508 | 2023 | Complications of Factor V Leiden in Adults Undergoing Noncardiac Surgical Procedures: A Systematic Review. | 0 |
| 37150682 | 2023 | [The analysis of a pedigree with hereditary coagulation factor Ⅴ deficiency caused by compound heterozygous variation of F5 gene]. | 1 |
| 37321256 | 2023 | Genetic Analysis of Hereditary Coagulation Factor V Deficiency in Two Chinese Families Caused by Compound Heterozygous Mutations. | 0 |
| 33993312 | 2023 | Stroke in Young Military Men With Heterozygous for MTHFR Gene Mutation or Factor V Leiden Gene Mutation Associated With Patent Foramen Ovale: Report of Two Cases and Therapeutic Strategy. | 1 |
Citation
Dessen P
F5 (coagulation factor V)
Atlas Genet Cytogenet Oncol Haematol. 2007-02-01
Online version: http://atlasgeneticsoncology.org/gene/45563/f5
