Acute Promyelocytic Leukemia([PML/RARalpha] and variants) Explore Disorder's Alias
An Unknown mode(s) within the Blood disorders category
Candidate Gene Information
An Unknown mode(s) within the Blood disorders category
Reported Pathogenic variants
S.No. | Name/GeneID | Description | Cytogentic Band | Gene Location on genomic DNA | Gene Length | Exons | Details | Gene Cross-References |
1 | RARA/5914 | retinoic acid receptor alpha | 17q21.2 | Chr17, NC_000017.11 (40309180..40357643) |
48464 nt | 17 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
2 | NUMA1/4926 | nuclear mitotic apparatus protein 1 | 11q13.4 | Chr11, NC_000011.10 (72002864..72080542, complement) |
77679 nt | 36 | More... | OMIM gene gnomAD browser EnsEMBL GeneCards ClinGen gene |
Variant Information | ||||||||
Disorder Cross-References: GARD GTR MalaCards NORD |
Patient care services
Clinical Symptoms & Disabilities
Prevalence
Under development |