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Browse result for Optic atrophy
※ introduction An optic nerve disease that is characterized the death of the retinal ganglion cell axons that comprise the optic nerve.
Reference
DiseaseOntology: Optic atrophy
Reference
DiseaseOntology: Optic atrophy
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD00450 | O00429 | 10059 | DNM1L | Dynamin-1-like protein | Homo sapiens |
| PTMD00786 | Q99798 | 50 | ACO2 | Aconitate hydratase, mitochondrial | Homo sapiens |
| PTMD02854 | O60313 | 4976 | OPA1 | Dynamin-like GTPase OPA1, mitochondrial [Cleaved into: Dynamin-like GTPase OPA1, long form ; Dynamin-like GTPase OPA1, short form ] | Homo sapiens |
| PTMD06214 | Q04837 | 6742 | SSBP1 | Single-stranded DNA-binding protein, mitochondrial | Homo sapiens |
| PTMD14866 | Q9Y4W6 | 10939 | AFG3L2 | Mitochondrial inner membrane m-AAA protease component AFG3L2 | Homo sapiens |