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Pathways
Genes search result for Homo sapiens
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4 records found for search term Wipf1
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
736993WIPF1WAS/WASL interacting protein family member 1This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction betw2174559574174682913Human234symbol , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
597621562WIPF1-AS1WIPF1 and CHRNA1 antisense RNA 12174575227174587726Humansymbol , COSMIC , name , Human Proteome Mapgene, ncrna, VALIDATED [RefSeq]
16556962AC010894.3novel transcript, antisense WIPF1Humannamegene, lncrna
16556532AC010894.2novel transcript, antisense to WIPF1 and CHRNA1Human1namegene, lncrna