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Browse result for hemolytic-uremic syndrome
※ introduction A kidney disease that is characterized by hemolytic anemia, thrombocytopenia, and renal failure caused by platelet thrombi in the microcirculation of the kidney and other organs.
Reference
DiseaseOntology: hemolytic-uremic syndrome
Reference
DiseaseOntology: hemolytic-uremic syndrome
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD01360 | P15529 | 4179 | CD46 | Membrane cofactor protein | Homo sapiens |
| PTMD03612 | P01024 | 718 | C3 | Complement C3 [Cleaved into: Complement C3 beta chain; C3-beta-c ; Complement C3 alpha chain; C3a anaphylatoxin; Acylation stimulating protein ; Complement C3b alpha' chain; Complement C3c alpha' chain fragment 1; Complement C3dg fragment; Complement C3g fragment; Complement C3d fragment; Complement C3f fragment; Complement C3c alpha' chain fragment 2] | Homo sapiens |
| PTMD03756 | P05156 | 3426 | CFI | Complement factor I [Cleaved into: Complement factor I heavy chain; Complement factor I light chain] | Homo sapiens |
| PTMD03885 | P08603 | 3075 | CFH | Complement factor H | Homo sapiens |
| PTMD05499 | P52429 | 8526 | DGKE | Diacylglycerol kinase epsilon | Homo sapiens |
| PTMD11193 | Q96EU7 | 29071 | C1GALT1C1 | C1GALT1-specific chaperone 1 | Homo sapiens |