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Browse result for Anemia
※ introduction A hematopoietic system disease that is characterized by a decrease in the normal number of red blood cells.
Reference
DiseaseOntology: Anemia
Reference
DiseaseOntology: Anemia
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD00530 | P11413 | 2539 | G6PD | Glucose-6-phosphate 1-dehydrogenase | Homo sapiens |
| PTMD01092 | P38646 | 3313 | HSPA9 | Stress-70 protein, mitochondrial | Homo sapiens |
| PTMD04525 | P22557 | 212 | ALAS2 | 5-aminolevulinate synthase, erythroid-specific, mitochondrial | Homo sapiens |
| PTMD06147 | Q02241 | 9493 | KIF23 | Kinesin-like protein KIF23 | Homo sapiens |
| PTMD06968 | Q15437 | 10483 | SEC23B | Protein transport protein Sec23B | Homo sapiens |
| PTMD08951 | Q86SX6 | 51218 | GLRX5 | Glutaredoxin-related protein 5, mitochondrial | Homo sapiens |
| PTMD09352 | Q8IWY9 | 14605 | CDAN1 | Codanin-1 | Homo sapiens |
| PTMD11144 | Q96DW6 | 54977 | SLC25A38 | Mitochondrial glycine transporter | Homo sapiens |
| PTMD12585 | Q9H0H5 | 29127 | RACGAP1 | Rac GTPase-activating protein 1 | Homo sapiens |
| PTMD14714 | Q9Y2V0 | 84529 | CDIN1 | CDAN1-interacting nuclease 1 | Homo sapiens |