About: WAS wt Allele     Goto   Sponge   NotDistinct   Permalink

An Entity of Type : owl:Class, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
rdfs:label
  • WAS wt Allele
equivalentClass
OMIM_Number
  • 300392
GenBank_Accession_Number
  • NM_000377
Semantic_Type
  • Gene or Genome
Preferred_Name
  • WAS wt Allele
UMLS_CUI
  • C1705616
EntrezGene_ID
  • 7454
Legacy_Concept_Name
  • WAS_wt_Allele
HGNC_ID
  • HGNC:12731
FULL_SYN
  • HPA3SYNCI
  • WAS wt AllelePTNCI
  • THCSYNCI
  • WASPSYNCI
  • Wiskott-Aldrich syndrome GeneSYNCI
  • Wiskott-Aldrich Syndrome (Eczema-Thrombocytopenia) wt AlleleSYNCI
Gene_Encodes_Product
  • Wiskott-Aldrich syndrome protein
DEFINITION
  • 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.NCI
code
  • C52261
Faceted Search & Find service v1.16.118 as of Jun 21 2024


Alternative Linked Data Documents: ODE     Content Formats:   [cxml] [csv]     RDF   [text] [turtle] [ld+json] [rdf+json] [rdf+xml]     ODATA   [atom+xml] [odata+json]     Microdata   [microdata+json] [html]    About   
This material is Open Knowledge   W3C Semantic Web Technology [RDF Data] Valid XHTML + RDFa
OpenLink Virtuoso version 07.20.3240 as of Jun 21 2024, on Linux (x86_64-pc-linux-gnu), Single-Server Edition (126 GB total memory, 48 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software