GenTIGSA Gene Database on Rare Genetic Disorders
  Beta Version

Lists of Rare Genetic Disorders      

Acute Lymphoid Leukemia(Acute lymphocytic leukemia) 
An Unknown mode(s) within the Cancer 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 FLT3/2322 fms related receptor tyrosine kinase 3 13q12.2 Chr13, NC_000013.11
(28003274..28100576, complement)
97303 nt 27 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

2 ETV6/2120 ETS variant transcription factor 6 12p13.2 Chr12, NC_000012.12
(11649674..11895377)
245704 nt 15 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

3 PAX5/5079 paired box 5 9p13.2 Chr9, NC_000009.12
(36833269..37034268, complement)
201000 nt 11 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

4 IKZF1/10320 IKAROS family zinc finger 1 7p12.2 Chr7, NC_000007.14
(50303455..50405101)
101647 nt 17 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

5 CDKN2A/1029 cyclin dependent kinase inhibitor 2A 9p21.3 Chr9, NC_000009.12
(21967752..21995324, complement)
27573 nt 10 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

Variant Information
Disorder Cross-References:      Orphanet          OMIM                    GTR          MedGen          MalaCards          EMBL-EBI OLS    Monarch Initiative          Human Phenotype Ontology          NORD     

Patient care services
Clinical Symptoms & Disabilities

Prevalence
Under development