WAS Chromosome X

WASP actin nucleation promoting factor
183 variants 183 Health Risk

Upload your DNA to see your personal genotypes for variants in WAS.

What This Gene Does
The Wiskott-Aldrich syndrome (WAS) family of proteins share similar domain structure, and are involved in transduction of signals from receptors on the cell surface to the actin cytoskeleton. The presence of a number of different motifs suggests that they are regulated by a number of different stimuli, and interact with multiple proteins. Recent studies have demonstrated that these proteins, directly or indirectly, associate with the small GTPase, Cdc42, known to regulate formation of actin filaments, and the cytoskeletal organizing complex, Arp2/3. Wiskott-Aldrich syndrome is a rare, inherited, X-linked, recessive disease characterized by immune dysregulation and microthrombocytopenia, and is caused by mutations in the WAS gene. The WAS gene product is a cytoplasmic protein, expressed exclusively in hematopoietic cells, which show signalling and cytoskeletal abnormalities in WAS patients. A transcript variant arising as a result of alternative promoter usage, and containing a different 5' UTR sequence, has been described, however, its full-length nature is not known. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Wiskott-Aldrich Syndrome protein family
Locus Type
gene with protein product
Location
Xp11.23
Ensembl
ENSG00000015285
Associated Conditions (17)
Inborn genetic diseases
Thrombocytopenia 1
Wiskott-Aldrich syndrome
X-linked severe congenital neutropenia
WAS-related disorder
WISKOTT-ALDRICH SYNDROME
ATTENUATED
Thrombocytopenia
THROMBOCYTOPENIA
X-LINKED
INTERMITTENT
Abnormality of blood and blood-forming tissues
Colon adenocarcinoma
Thyroid cancer
nonmedullary
1
X-Linked Neutropenia
Key Variants
RS1186676831
Conflicting classifications of pathogenicity
Inborn genetic diseases, Thrombocytopenia 1, Wiskott-Aldrich syndrome
Health Risk
RS1307143057
Conflicting classifications of pathogenicity
X-linked severe congenital neutropenia, Wiskott-Aldrich syndrome, Thrombocytopenia 1
Health Risk
RS139857045
Conflicting classifications of pathogenicity
Thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia
Health Risk
RS1409607754
Conflicting classifications of pathogenicity
X-linked severe congenital neutropenia, Wiskott-Aldrich syndrome, Thrombocytopenia 1
Health Risk
RS1440423616
Conflicting classifications of pathogenicity
X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
Health Risk
RS145040665
Conflicting classifications of pathogenicity
Thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia
Health Risk
RS146220228
Conflicting classifications of pathogenicity
X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
Health Risk
RS149932808
Conflicting classifications of pathogenicity
Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia, Thrombocytopenia 1
Health Risk
RS1569494034
Conflicting classifications of pathogenicity
Thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia
Health Risk
RS193922412
Conflicting classifications of pathogenicity
Wiskott-Aldrich syndrome, Thrombocytopenia 1, X-linked severe congenital neutropenia
Health Risk
RS200261212
Conflicting classifications of pathogenicity
Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia, Thrombocytopenia 1
Health Risk
RS201657175
Conflicting classifications of pathogenicity
X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
Health Risk
All Variants (183)
RSID Category Clinical Significance Conditions
RS1186676831 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Thrombocytopenia 1, Wiskott-Aldrich syndrome
RS1307143057 Health Risk Conflicting classifications of pathogenicity X-linked severe congenital neutropenia, Wiskott-Aldrich syndrome, Thrombocytopenia 1
RS139857045 Health Risk Conflicting classifications of pathogenicity Thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia
RS1409607754 Health Risk Conflicting classifications of pathogenicity X-linked severe congenital neutropenia, Wiskott-Aldrich syndrome, Thrombocytopenia 1
RS1440423616 Health Risk Conflicting classifications of pathogenicity X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
RS145040665 Health Risk Conflicting classifications of pathogenicity Thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia
RS146220228 Health Risk Conflicting classifications of pathogenicity X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
RS149932808 Health Risk Conflicting classifications of pathogenicity Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia, Thrombocytopenia 1
RS1569494034 Health Risk Conflicting classifications of pathogenicity Thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia
RS193922412 Health Risk Conflicting classifications of pathogenicity Wiskott-Aldrich syndrome, Thrombocytopenia 1, X-linked severe congenital neutropenia
RS200261212 Health Risk Conflicting classifications of pathogenicity Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia, Thrombocytopenia 1
RS201657175 Health Risk Conflicting classifications of pathogenicity X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
RS35359501 Health Risk Conflicting classifications of pathogenicity Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia, Thrombocytopenia 1
RS373524969 Health Risk Conflicting classifications of pathogenicity Thrombocytopenia 1, X-linked severe congenital neutropenia, Wiskott-Aldrich syndrome
RS374283590 Health Risk Conflicting classifications of pathogenicity Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia, Thrombocytopenia 1
RS376560886 Health Risk Conflicting classifications of pathogenicity Thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia
RS781799471 Health Risk Conflicting classifications of pathogenicity X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
RS782115211 Health Risk Conflicting classifications of pathogenicity Thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia
RS782158640 Health Risk Conflicting classifications of pathogenicity X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
RS782195195 Health Risk Conflicting classifications of pathogenicity X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
RS782224455 Health Risk Conflicting classifications of pathogenicity Thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia
RS782307200 Health Risk Conflicting classifications of pathogenicity Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia, Thrombocytopenia 1
RS782415042 Health Risk Conflicting classifications of pathogenicity X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
RS782420124 Health Risk Conflicting classifications of pathogenicity Thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia
RS782584950 Health Risk Conflicting classifications of pathogenicity WAS-related disorder, X-linked severe congenital neutropenia, Thrombocytopenia 1
RS782596670 Health Risk Conflicting classifications of pathogenicity Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia, Thrombocytopenia 1
RS782602857 Health Risk Conflicting classifications of pathogenicity Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia, Thrombocytopenia 1
RS782631956 Health Risk Conflicting classifications of pathogenicity Thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia
RS782636781 Health Risk Conflicting classifications of pathogenicity Thrombocytopenia 1, Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia
RS782666797 Health Risk Conflicting classifications of pathogenicity X-linked severe congenital neutropenia, Wiskott-Aldrich syndrome, Thrombocytopenia 1
RS782730988 Health Risk Conflicting classifications of pathogenicity X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
RS782761074 Health Risk Conflicting classifications of pathogenicity Wiskott-Aldrich syndrome, X-linked severe congenital neutropenia, Thrombocytopenia 1
RS868970795 Health Risk Conflicting classifications of pathogenicity X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
RS132630268 Health Risk Likely pathogenic Wiskott-Aldrich syndrome, Wiskott-Aldrich syndrome, Thrombocytopenia 1
RS132630272 Health Risk Likely pathogenic WISKOTT-ALDRICH SYNDROME, ATTENUATED, WISKOTT-ALDRICH SYNDROME
RS132630273 Health Risk Likely pathogenic Thrombocytopenia 1, Thrombocytopenia, Wiskott-Aldrich syndrome
RS132630275 Health Risk Likely pathogenic THROMBOCYTOPENIA, X-LINKED, INTERMITTENT
RS1557006316 Health Risk Likely pathogenic
RS1557006474 Health Risk Likely pathogenic Wiskott-Aldrich syndrome, Wiskott-Aldrich syndrome
RS1557006534 Health Risk Likely pathogenic Wiskott-Aldrich syndrome, Wiskott-Aldrich syndrome
RS1557006672 Health Risk Likely pathogenic Wiskott-Aldrich syndrome, Wiskott-Aldrich syndrome
RS1557007035 Health Risk Likely pathogenic Wiskott-Aldrich syndrome, Wiskott-Aldrich syndrome
RS1602180020 Health Risk Likely pathogenic
RS193922414 Health Risk Likely pathogenic Wiskott-Aldrich syndrome, Wiskott-Aldrich syndrome
RS193922416 Health Risk Likely pathogenic Wiskott-Aldrich syndrome, Wiskott-Aldrich syndrome
RS2062412197 Health Risk Likely pathogenic X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
RS2062418811 Health Risk Likely pathogenic Wiskott-Aldrich syndrome, Wiskott-Aldrich syndrome
RS2062426981 Health Risk Likely pathogenic X-linked severe congenital neutropenia, Thrombocytopenia 1, Wiskott-Aldrich syndrome
RS2147262523 Health Risk Likely pathogenic Wiskott-Aldrich syndrome, Wiskott-Aldrich syndrome
RS2147262778 Health Risk Likely pathogenic
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