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- NCIT_C52261 IAO_0000115 "Human WAS wild-type allele is located within Xp11.4-p11.21 and is approximately 8 kb in length. This allele, which encodes Wiskott-Aldrich syndrome protein, plays a role in actin cytoskeletal organization. Mutations in this gene are the cause of Wiskott-Aldrich syndrome an X-linked disease characterized by eczema, immune deficiencies and thrombocytopenia." @default.
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- NCIT_C52261 NCIT_P106 "Gene or Genome" @default.
- NCIT_C52261 NCIT_P107 "WAS wt Allele" @default.
- NCIT_C52261 NCIT_P108 "WAS wt Allele" @default.
- NCIT_C52261 NCIT_P207 "C1705616" @default.
- NCIT_C52261 NCIT_P321 "7454" @default.
- NCIT_C52261 NCIT_P322 "CTRP" @default.
- NCIT_C52261 NCIT_P366 "WAS_wt_Allele" @default.
- NCIT_C52261 NCIT_P96 "Wiskott-Aldrich syndrome protein" @default.
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- NCIT_C52261 hasExactSynonym "IMD2" @default.
- NCIT_C52261 hasExactSynonym "THC" @default.
- NCIT_C52261 hasExactSynonym "WAS wt Allele" @default.
- NCIT_C52261 hasExactSynonym "WASP" @default.
- NCIT_C52261 hasExactSynonym "Wiskott-Aldrich Syndrome (Eczema-Thrombocytopenia) wt Allele" @default.
- NCIT_C52261 hasExactSynonym "Wiskott-Aldrich syndrome Gene" @default.
- NCIT_C52261 inSubset NCIT_C116977 @default.
- NCIT_C52261 inSubset NCIT_C142799 @default.
- NCIT_C52261 inSubset NCIT_C142800 @default.
- NCIT_C52261 type Class @default.
- NCIT_C52261 isDefinedBy ncit.owl @default.
- NCIT_C52261 label "WAS wt Allele" @default.
- NCIT_C52261 subClassOf NCIT_C16612 @default.
- NCIT_C52261 subClassOf NCIT_C20194 @default.
- NCIT_C52261 subClassOf NCIT_C43236 @default.
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