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Browse result for Pelger-Huet anomaly
※ introduction A hematopoietic system disease characterized by white blood cells with unusually shaped nuclei that has_material_basis_in heterozygous mutation in LBR on chromosome 1q42.12.
Reference
DiseaseOntology: Pelger-Huet anomaly
Reference
DiseaseOntology: Pelger-Huet anomaly
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD06809 | Q14739 | 3930 | LBR | Delta-sterol reductase LBR -reductase) | Homo sapiens |