GenTIGSA Gene Database on Rare Genetic Disorders
  Beta Version

Lists of Rare Genetic Disorders  

Wiskott-Aldrich Syndrome(Wiskott Aldrich syndrome)      Explore Disorder's Alias
An X-linked dominant mode(s) within the Immune 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 WAS/7454 WASP actin nucleation promoting factor Xp11.23 ChrX, NC_000023.11
(48676636..48691427)
14792 nt 13 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

2 WIPF1/7456 WAS/WASL interacting protein family member 1 2q31.1 Chr2, NC_000002.12
(174559574..174682913, complement)
123340 nt 18 More... OMIM gene
gnomAD browser
EnsEMBL
GeneCards
ClinGen gene

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

Patient care services
Clinical Symptoms & Disabilities

Prevalence
Under development