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: 2155
MIM: 613878
HGNC: 3544
Ensembl: ENSG00000057593
Variants:
dbSNP: 2155
ClinVar: 2155
TCGA: ENSG00000057593
COSMIC: F7
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000057593 | ENST00000346342 | P08709 |
| ENSG00000057593 | ENST00000375581 | P08709 |
| ENSG00000057593 | ENST00000444337 | E9PH36 |
| ENSG00000057593 | ENST00000541084 | F5H8B0 |
Expression (GTEx)
Pathways
PharmGKB
| Entity ID | Name | Type | Evidence | Association | PK | PD | PMIDs |
|---|---|---|---|---|---|---|---|
| PA28660 | GGCX | Gene | Pathway | associated |
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38335567 | 2024 | Frequency of the p.Thr241Asn mutation in Chinese patients with congenital factor VII deficiency. | 0 |
| 38926980 | 2024 | [Congenital FⅦ Deficiency Associated with a Novel Mutation in F7 Gene]. | 0 |
| 38926981 | 2024 | [Pedigree Analysis of Hereditary Coagulation Factor XII Deficiency Caused by Compound Heterozygous Mutation p.Gly175Cys and p.Gly542Ser of F12 Gene]. | 0 |
| 38335567 | 2024 | Frequency of the p.Thr241Asn mutation in Chinese patients with congenital factor VII deficiency. | 0 |
| 38926980 | 2024 | [Congenital FⅦ Deficiency Associated with a Novel Mutation in F7 Gene]. | 0 |
| 38926981 | 2024 | [Pedigree Analysis of Hereditary Coagulation Factor XII Deficiency Caused by Compound Heterozygous Mutation p.Gly175Cys and p.Gly542Ser of F12 Gene]. | 0 |
| 36719811 | 2023 | Factor VII Padua in Iran: clinical and laboratory findings of three unrelated patients. | 1 |
| 36951360 | 2023 | Structural and functional characterization of novel F7 mutations identified in Chinese factor VII-deficient patients. | 1 |
| 37042485 | 2023 | Factor VII deficiency: A cause of (or risk factor for) bleeding? | 0 |
| 37993374 | 2023 | Acquired factor VII deficiency in pediatric inflammatory bowel disease: Report of three cases. | 0 |
| 36719811 | 2023 | Factor VII Padua in Iran: clinical and laboratory findings of three unrelated patients. | 1 |
| 36951360 | 2023 | Structural and functional characterization of novel F7 mutations identified in Chinese factor VII-deficient patients. | 1 |
| 37042485 | 2023 | Factor VII deficiency: A cause of (or risk factor for) bleeding? | 0 |
| 37993374 | 2023 | Acquired factor VII deficiency in pediatric inflammatory bowel disease: Report of three cases. | 0 |
| 34469511 | 2022 | Factor VIIa suppresses inflammation and barrier disruption through the release of EEVs and transfer of microRNA 10a. | 10 |
Citation
Dessen P
F7 (coagulation factor VII)
Atlas Genet Cytogenet Oncol Haematol. 2007-02-01
Online version: http://atlasgeneticsoncology.org/gene/46526/f7
