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Browse result for Rod-cone dystrophy
※ introduction A cone dystrophy is an inherited ocular disorder characterized by the loss of cone cells, the photoreceptors responsible for both central and color vision.
Reference
Wiki: Rod-cone dystrophy
Reference
Wiki: Rod-cone dystrophy
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD03155 | O75643 | 23020 | SNRNP200 | U5 small nuclear ribonucleoprotein 200 kDa helicase | Homo sapiens |
| PTMD04452 | P20839 | 3614 | IMPDH1 | Inosine-5'-monophosphate dehydrogenase 1 | Homo sapiens |
