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Browse result for Antley-Bixler syndrome
※ introduction Antley¨CBixler syndrome is a rare, severe autosomal recessive congenital disorder characterized by malformations and deformities affecting the majority of the skeleton and other areas of the body.
Reference
Wiki: Antley-Bixler syndrome
Reference
Wiki: Antley-Bixler syndrome
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD01009 | P21802 | 2263 | FGFR2 | Fibroblast growth factor receptor 2 | Homo sapiens |
| PTMD04277 | P16435 | 5447 | POR | NADPH--cytochrome P450 reductase | Homo sapiens |
