GenTIGSA Gene Database on Rare Genetic Disorders
  Beta Version

Lists of Rare Genetic Disorders  

Acute Promyelocytic Leukemia([PML/RARalpha] and variants)      Explore Disorder's Alias
An Unknown mode(s) within the Blood disorders category
Reported Pathogenic variants
Candidate Gene Information
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