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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
platelet-type bleeding disorder 17
Summary
- Synonym
-
- BDPLT17
- hereditary thrombasthenia-thrombocytopenia
- Definition
- A blood platelet disease characterized by autosomal dominant inheritance of increased bleeding tendency, gray platelets, thrombocytopenia, thrombasthenia, abnormal megakaryocytes, decreased or absent alpha-granules in platelets, and myelofibrosis that has_material_basis_in heterozygous mutation in the GFI1B gene on chromosome 9q34.
- Super Class
- autosomal dominant disease blood platelet disease
External Links
- Disease Ontology
- DOID:0111049
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- OMIM
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P09382 | Galectin-1 | |
| P09622 | Dihydrolipoyl dehydrogenase, mitochondrial | |
| P14555 | Phospholipase A2, membrane associated | |
| P16109 | P-selectin | |
| P19320 | Vascular cell adhesion protein 1 | |
| P54802 | Alpha-N-acetylglucosaminidase | |
| Q02083 | N-acylethanolamine-hydrolyzing acid amidase | |
| Q8WWQ2 | Inactive heparanase-2 | |
| Q9Y251 | Heparanase |
