rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiency.
10447256
1999
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Identification of 19 protein S gene mutations in patients with phenotypic protein S deficiency and thrombosis. Protein S Study Group.
8943854
1996
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Identification of eight point mutations in protein S deficiency type I--analysis of 15 pedigrees.
7482398
1995
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Protein S deficiency type I: identification of point mutations in 9 of 10 families.
7579449
1995
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Protein S Tokushima: abnormal molecule with a substitution of Glu for Lys-155 in the second epidermal growth factor-like domain of protein S.
8298131
1994
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Optimization of a simple and rapid single-strand conformation analysis for detection of mutations in the PROS1 gene: identification of seven novel mutations and three novel, apparently neutral, variants.
10790208
2000
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S.
10706858
2000
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Poor relationship between phenotypes of protein S deficiency and mutations in the protein S alpha gene.
10613647
1999
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Genetic and phenotypic variability between families with hereditary protein S deficiency.
11858485
2002
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Protein S Gla-domain mutations causing impaired Ca(2+)-induced phospholipid binding and severe functional protein S deficiency.
12351389
2002
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Functional characterization of twelve natural PROS1 mutations associated with anticoagulant protein S deficiency.
18322254
2008
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
The management of depression during pregnancy: a report from the American Psychiatric Association and the American College of Obstetricians and Gynecologists.
20027064
2010
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies.
8765219
1996
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene.
7803790
1995
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Four missense mutations identified in the protein S gene of thrombosis patients with protein S deficiency: effects on secretion and anticoagulant activity of protein S.
11927129
2002
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations.
12632031
2003
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Identification of three novel mutations in hereditary protein S deficiency.
9031443
1997
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Molecular basis of protein S deficiency in three families also showing independent inheritance of factor V leiden.
8781426
1996
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Identification of two novel point mutations in the human protein S gene associated with familial protein S deficiency and thrombosis.
8977443
1996
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Characterization and structural impact of five novel PROS1 mutations in eleven protein S-deficient families.
11776305
2001
rs121918473
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Five novel mutations of the protein S active gene (PROS 1) in 8 Norman families.
8701404
1996
rs121918474
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Five novel mutations of the protein S active gene (PROS 1) in 8 Norman families.
8701404
1996
rs121918474
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Protein S Gla-domain mutations causing impaired Ca(2+)-induced phospholipid binding and severe functional protein S deficiency.
12351389
2002
rs121918474
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Functional characterization of twelve natural PROS1 mutations associated with anticoagulant protein S deficiency.
18322254
2008
rs121918474
×
Entrez Id:
5627
Gene Symbol:
PROS1
PROS1
THROMBOPHILIA DUE TO PROTEIN S DEFICIENCY, AUTOSOMAL DOMINANT
0.800
GeneticVariation
UNIPROT
Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies. The French Network on Molecular Abnormalities Responsible for Protein C and Protein S Deficiencies.
8765219
1996