PROS1
is a | gene |
is | mentioned by |
ClinVar | PROS1 |
GeneCards | PROS1 |
Diseases | PROS1 |
wikipedia | PROS1 |
PROS1 | |
gopubmed | PROS1 |
EVS | PROS1 |
HEFalMp | PROS1 |
MyGene2 | PROS1 |
23andMe | PROS1 |
# SNPs | 39 |
Max Magnitude | Chromosome position | Summary | |
---|---|---|---|
i5005055 | |||
i5005056 | |||
i5005058 | |||
i5005059 | |||
rs1131691605 | 5 | 93,886,504 | |
rs121918472 | 6 | 93,879,306 | |
rs121918473 | 5 | 93,898,524 | |
rs121918474 | 5 | 93,905,799 | |
rs121918475 | 5 | 93,898,462 | |
rs121918476 | 5 | 93,877,155 | |
rs138925964 | 6 | 93,879,279 | |
rs199469484 | 0 | 93,973,917 | |
rs199469485 | 0 | 93,927,331 | |
rs199469486 | 0 | 93,910,693 | |
rs199469487 | 0 | 93,905,802 | |
rs199469488 | 0 | 93,896,676 | |
rs199469489 | 0 | 93,896,773 | |
rs199469490 | 0 | 93,893,139 | |
rs199469491 | 0 | 93,892,993 | |
rs199469492 | 0 | 93,892,933 | |
rs199469493 | 0 | 93,893,186 | |
rs199469494 | 0 | 93,892,928 | |
rs199469495 | 0 | 93,886,430 | |
rs199469496 | 0 | 93,884,827 | |
rs199469497 | 0 | 93,905,784 | |
rs199469498 | 0 | 93,884,730 | |
rs199469499 | 0 | 93,884,782 | |
rs199469500 | 0 | 93,879,264 | |
rs199469501 | 0 | 93,879,331 | |
rs199469502 | 0 | 93,879,091 | |
rs199469503 | 0 | 93,877,156 | |
rs267606981 | 5 | 93,874,245 | |
rs368074804 | 5 | 93,898,570 | |
rs387906674 | 5 | 93,893,025 | |
rs387906675 | 9 | 93,900,830 | |
rs4857037 | 0 | 93,908,968 | |
rs5017717 | 0 | 93,884,869 | |
rs6122 | 5 | 93,927,251 | |
rs863224838 | 5 | 93,893,121 |
From: Genetics Home Reference
The PROS1 gene provides instructions for making a protein called protein S that is important for controlling blood clotting. By itself, protein S cannot carry out the chemical reactions necessary for regulating the formation of blood clots. Instead, protein S attaches to certain enzymes and enhances their function. On the basis of this action, protein S is called a cofactor.
Protein S is made chiefly by cells in the liver. The protein circulates in the bloodstream in two forms; it is either attached (bound) to a specific protein or occurs by itself in a free form. Both forms of proteins S can act as cofactors; however, bound protein S is less effective than the free form. Protein S is a cofactor for an enzyme called activated protein C (APC). APC turns off (inactivates) the blood clotting proteins known as factor Va and factor VIIIa. Protein S also helps an enzyme known as tissue factor pathway inhibitor (TFPI) block the activity of another clotting protein, factor Xa.
More than 220 mutations in the PROS1 gene have been found to cause protein S deficiency. Most of these mutations change single protein building blocks (amino acids) in protein S, which disrupts its ability to act as a cofactor. Protein S deficiency can be divided into three types based on the mutation in the PROS1 gene.
Protein S deficiency type I is caused by PROS1 gene mutations that result in reduced levels of protein S. Affected individuals do not have enough protein S to control blood clotting, which causes the increased risk for abnormal blood clots in protein S deficiency.
Mutations that cause protein S deficiency type II result in the production of an altered protein S with reduced activity. Individuals with this form of the condition have normal levels of protein S, but the protein is not able to interact with other molecules involved in blood clotting. If protein S does not function properly, abnormal blood clots may form.
Protein S deficiency type III occurs when there is a low amount of free protein S, but the overall amount of protein S is normal. Because free protein S is a more effective cofactor than bound protein S, reduced levels of free protein S can disrupt the inactivation of blood clotting proteins.
Diseases associated with PROS1 include thrombophilia due to Protein S deficiency, which is can be inherited in either an autosomal dominant or recessive manner.OMIM
Genotypes in SNPedia that containing pathogenic PROS1 gene mutations may include reference to the ClinGen Actionability PROS1 page, which is based on thrombophilia due to protein S deficiency.