|Dataset||MPO Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||aberrant levels of the antihemophilic factor that is part of the factor VIII/von Willebrand factor complex; it is produced in the liver and acts in the intrinsic pathway of blood coagulation; it serves as a cofactor in factor X activation and this action is markedly enhanced by small amounts of thrombin (Mammalian Phenotype Ontology, MP_0012327)|
|Downloads & Tools|
1 gene mutations causing the abnormal circulating factor viii level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
|MGAT4B||mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase, isozyme B|