rs121918028
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.810 |
GeneticVariation |
BEFREE |
Three types of mutations (Ala601Thr, Val355Phe, and Asp676Asn) have been described in dysplasminogenemia.
|
12692411 |
2003 |
rs121918028
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.810 |
GeneticVariation |
UNIPROT |
Compound-heterozygous mutations in the plasminogen gene predispose to the development of ligneous conjunctivitis.
|
10233898 |
1999 |
rs121918028
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.810 |
GeneticVariation |
UNIPROT |
Plasminogen Kanagawa-I, a novel missense mutation, is caused by the amino acid substitution G732R.
|
9858247 |
1998 |
rs121918028
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.810 |
GeneticVariation |
UNIPROT |
Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitis.
|
9242524 |
1997 |
rs121918028
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.810 |
GeneticVariation |
UNIPROT |
Congenital plasminogen deficiency caused by a Ser572 to Pro mutation.
|
8392398 |
1993 |
rs121918028
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.810 |
GeneticVariation |
UNIPROT |
Plasminogen with type-I mutation is polymorphic in the Japanese population.
|
1427790 |
1992 |
rs121918028
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.810 |
GeneticVariation |
UNIPROT |
Two types of abnormal genes for plasminogen in families with a predisposition for thrombosis.
|
1986355 |
1991 |
rs121918028
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.810 |
GeneticVariation |
UNIPROT |
Plasminogens Tochigi II and Nagoya: two additional molecular defects with Ala-600----Thr replacement found in plasmin light chain variants.
|
6238949 |
1984 |
rs121918028
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.810 |
GeneticVariation |
UNIPROT |
Plasminogen Tochigi: inactive plasmin resulting from replacement of alanine-600 by threonine in the active site.
|
6216475 |
1982 |
rs121918028
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
T |
0.810 |
CausalMutation |
CLINVAR |
|
|
|
rs73015965
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
G |
0.800 |
GeneticVariation |
CLINVAR |
Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.
|
31064749 |
2019 |
rs121918029
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Compound-heterozygous mutations in the plasminogen gene predispose to the development of ligneous conjunctivitis.
|
10233898 |
1999 |
rs121918030
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Compound-heterozygous mutations in the plasminogen gene predispose to the development of ligneous conjunctivitis.
|
10233898 |
1999 |
rs121918033
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Compound-heterozygous mutations in the plasminogen gene predispose to the development of ligneous conjunctivitis.
|
10233898 |
1999 |
rs121918029
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Plasminogen Kanagawa-I, a novel missense mutation, is caused by the amino acid substitution G732R.
|
9858247 |
1998 |
rs121918030
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Plasminogen Kanagawa-I, a novel missense mutation, is caused by the amino acid substitution G732R.
|
9858247 |
1998 |
rs121918033
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Plasminogen Kanagawa-I, a novel missense mutation, is caused by the amino acid substitution G732R.
|
9858247 |
1998 |
rs121918029
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitis.
|
9242524 |
1997 |
rs121918030
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitis.
|
9242524 |
1997 |
rs121918033
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Homozygous mutations in the plasminogen gene of two unrelated girls with ligneous conjunctivitis.
|
9242524 |
1997 |
rs121918029
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Congenital plasminogen deficiency caused by a Ser572 to Pro mutation.
|
8392398 |
1993 |
rs121918030
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Congenital plasminogen deficiency caused by a Ser572 to Pro mutation.
|
8392398 |
1993 |
rs121918033
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Congenital plasminogen deficiency caused by a Ser572 to Pro mutation.
|
8392398 |
1993 |
rs121918029
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Plasminogen with type-I mutation is polymorphic in the Japanese population.
|
1427790 |
1992 |
rs121918030
|
Entrez Id: |
5340 |
Gene Symbol: |
PLG |
PLG
|
Plasminogen Deficiency, Type I
|
|
0.800 |
GeneticVariation |
UNIPROT |
Plasminogen with type-I mutation is polymorphic in the Japanese population.
|
1427790 |
1992 |