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Human Disease and Mouse Model Detail
Human Disease Scott Syndrome; SCTS
OMIM ID: 262890
Human Phenotype Ontology associations
Synonyms Bleeding Abnormality Due to Deficiency of Platelet Binding of Factor X; Bleeding Disorder, Platelet-Type; Bleeding Disorder, Platelet-Type, 7; BDPLT7; Prothrombin Consumption Deficiency; Prothrombin Consumption Inhibitor, Familial; Prothrombin Conversion Defect, Familial
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     ANO6* Ano6   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory