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Browse result for Microphthalmia
※ introduction An eye disease where one or both eyeballs are abnormally small.
Reference
DiseaseOntology: Microphthalmia
Reference
DiseaseOntology: Microphthalmia
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD00056 | P48431 | 6657 | SOX2 | Transcription factor SOX-2 | Homo sapiens |
| PTMD04050 | P10826 | 5915 | RARB | Retinoic acid receptor beta | Homo sapiens |
| PTMD04121 | P12644 | 652 | BMP4 | Bone morphogenetic protein 4 | Homo sapiens |
| PTMD05206 | P47895 | 220 | ALDH1A3 | Retinaldehyde dehydrogenase 3 | Homo sapiens |
| PTMD05726 | P58304 | 33891 | VSX2 | Visual system homeobox 2 | Homo sapiens |
| PTMD08471 | Q6W2J9 | 54880 | BCOR | BCL-6 corepressor | Homo sapiens |
| PTMD12267 | Q9BX79 | 64220 | STRA6 | Receptor for retinol uptake STRA6 | Homo sapiens |
| PTMD13903 | Q9P273 | 55714 | TENM3 | Teneurin-3 | Homo sapiens |
| PTMD14894 | Q9Y586 | 10586 | MAB21L2 | Protein mab-21-like 2 | Homo sapiens |