OMIA group 1353
Scott syndrome
The chain reaches the human disease Scott syndrome, which Mondo defines as: “A blood coagulation disorder caused by a variant in the ANO6 gene, characterized by impaired externalization of phosphatidylserine on activated platelets, resulting in a reduced procoagulant platelet surface, diminished thrombin generation, and mucocutaneous bleeding. Platelet counts and morphology are generally normal, but affected individuals show markedly reduced platelet procoagulant activity with defective membrane scrambling in response to calcium‑dependent stimuli.”
The chain
From the animal disease to the drugs. The page shows what each step found and where the chain stopped. It does not say whether the animal is a model of a human disease.
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Animal disease
Reached
OMIA records it in 1 species entry marked as a defect.
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Human disease
Reached
1 Mondo disease.
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Human gene
Reached
1 human gene.
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Target evidence
Reached
1 Open Targets association, with a best score of 0.71.
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Drugs
Stopped here
No ChEMBL drug acts on a human gene of the group's target evidence.
The chain stopped at Drugs: No ChEMBL drug acts on a human gene of the group's target evidence.
Natural-model score
How complete and how well supported the chain to each human disease is, out of 100, by stated rules. It does not say that the animal is a validated model of the human disease. How the score works.
59.0 out of 100
| Part | Computed from | Points |
|---|---|---|
| Target evidence | Open Targets score of 0.71 | 25.0 of 35 |
| Drugs | No drug has been tested for this disease, and none acts on its genes | 0.0 of 25 |
| Ortholog | One to one ortholog | 20.0 of 20 |
| Both routes | Both routes found this disease | 10.0 of 10 |
| Species | 1 naturally occurring species entry marked as a defect | 4.0 of 10 |
Species
The chain follows only the species entries that OMIA marks as a defect.
| Species | Scientific name | OMIA entry | A defect |
|---|---|---|---|
| dog | Canis lupus familiaris | OMIA:001353-9615 | Yes |
Genes
Each gene OMIA records for a species entry, and the human gene it reaches through Ensembl's orthologs.
| Species | Animal gene | Human gene | Ortholog |
|---|---|---|---|
| dog | ANO6 anoctamin 6 NCBI Gene 486597 | ANO6 Ensembl | one to one |
Human diseases
Two routes lead from an OMIA group to a Mondo human disease: OMIA's own Mondo link, and the group's OMIM numbers through Mondo's cross-references.
- OMIA's own Mondo link: found a disease.
- OMIA's OMIM numbers: found a disease.
| Mondo disease | Name | Found by |
|---|---|---|
| MONDO:0009885 | Scott syndrome A blood coagulation disorder caused by a variant in the ANO6 gene, characterized by impaired externalization of phosphatidylserine on activated platelets, resulting in a reduced procoagulant platelet surface, diminished thrombin generation, and mucocutaneous bleeding. Platelet counts and morphology are generally normal, but affected individuals show markedly reduced platelet procoagulant activity with defective membrane scrambling in response to calcium‑dependent stimuli. | Both routes |
Target evidence
Each Open Targets association between one of the group's human genes and one of its human diseases, with its overall score and the score for each kind of evidence.
| Human gene | Human disease | Score | Evidence | Kinds of evidence |
|---|---|---|---|---|
| ANO6 | Scott syndrome | 0.71 | 87 | Genetic association 0.81 Genetic literature 0.70 Literature 0.14 |
Drugs
No ChEMBL drug acts on a human gene of the group's target evidence.