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Browse result for Keratoconus
※ introduction A corneal disease characterized by structural changes within the cornea causing it to thin and change, leading to a protruding conical shape.
Reference
DiseaseOntology: Keratoconus
Reference
DiseaseOntology: Keratoconus
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD00094 | Q16236 | 4780 | NFE2L2 | Nuclear factor erythroid 2-related factor 2 | Homo sapiens |
| PTMD01580 | P29033 | 2706 | GJB2 | Gap junction beta-2 protein | Homo sapiens |
| PTMD03896 | P08779 | 3868 | KRT16 | Keratin, type I cytoskeletal 16 | Homo sapiens |
| PTMD05615 | P55064 | 362 | AQP5 | Aquaporin-5 | Homo sapiens |
| PTMD13809 | Q9NZR4 | 30813 | VSX1 | Visual system homeobox 1 | Homo sapiens |