Links : Database Haemostaseology - Factor VII
Factor VII
-
DHPLC Melt Programm
[A method generally successful at separating DNA duplexes that differ in the identity of one or more base pairs.]
-
Factor VII and VII a
[Factor VII is the zymogen form (inactive precursor), and factor VIIa is the active enzyme form (serine protease).]
-
GeneCard for gene F7GC13P112846
[Chromosome: 13 GeneLoc gene densities LocusLink cytogenetic band: 13q34 Ensembl cytogenetic band: 13q34]
-
Human Gene Mutation Database Cardiff (HGMD)
[Mutations in Gene symbol: F7, Factor VII Location : 13q34]
-
Molekularpathologie des hereditären Faktor VII Mangels
[Aufklärung von FVII Genmutationen durch DNA-Sequenzierung, molekulare Struktur-Funktionsanalyse und vergleichende Struktur-Funktion-Analysen]
- MRC Haemostasis & Thrombosis Database Resource Sites
[Provides links to HAMSTeRS, CoagBase and Factor VII Databeses]
-
NCBI Sequence Viewer
[AF466933[gi:18251977] Homo sapiens coagulation factor VII (serum prothrombin conversion accelerator) (F7) gene, complete cds.]
-
NCBI Sequence Viewer
[NT_027140[gi:18596849] Homo sapiens chromosome 13 genomic contig.]
-
NCBI Sequence Viewer
[J02933. Human blood coagu...[gi:180333] Human blood coagulation factor VII gene, complete cds.]
-
NCBI Sequence Viewer
[NT_027140[gi:18596849] Homo sapiens chromosome 13 genomic contig]
-
NCBI Sequence Viewer
[NM_000131[gi:10518501] Homo sapiens coagulation factor VII (serum prothrombin conversion accelerator) (F7), transcript variant 1, mRNA.]
-
NCBI Sequence Viewer
[NM_019616[gi:10518502] Homo sapiens coagulation factor VII (serum prothrombin conversion accelerator) (F7), transcript variant 2, mRNA.]
-
Single Nucleotide Polymorphism
[Gene Model (mRNA alignment) information from genome sequence]
-
Swiss-Prot: of P08709
[FA7_HUMAN P08709]
-
Trigger (an electronic newsletter for researchers working on the biology of Tissue Factor, Factor VII and TFPI).
[X-ray Crystal Structures and NMR Structures of Tissue Factor, Factor VII, Factor VIIa, and TFPI]
-
Whitehead Institute for Biomedical Research/MIT Center for Genome Research
[Whitehead cSNP Data]
-
*277450 Vitamin K-dependent Clotting factors
[A genetic disorder of vitamin K metabolism might lead to a congenital combined deficiency of Prothrombin, Stuart factor, factor VII and Christmas factor.]
