abnormal circulating antithrombin level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant blood level of the family of glycoproteins which neutralize the ability of thrombin to promote blood coagulation (Mammalian Phenotype Ontology, MP_0012324)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012324
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1 gene mutations causing the abnormal circulating antithrombin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
TXNIP thioredoxin interacting protein