WASF2 WASP family member 2 [ Homo sapiens (human) ]
Source: NCBI Gene (ID 10163)
Symbol: WASF2
Full name: WASP family member 2
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Also known as: IMD2; SCAR2; WASF4; WAVE2; dJ393P12.2
Summary: This gene encodes a member of the Wiskott-Aldrich syndrome protein family. The gene product is a protein that forms a multiprotein complex that links receptor kinases and actin. Binding to actin occurs through a C-terminal verprolin homology domain in all family members. The multiprotein complex serves to tranduce signals that involve changes in cell shape, motility or function. The published map location (PMID:10381382) has been changed based on recent genomic sequence comparisons, which indicate that the expressed gene is located on chromosome 1, and a pseudogene may be located on chromosome X. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]
Expression: Ubiquitous expression in esophagus (RPKM 43.4), ovary (RPKM 33.8) and 25 other tissues
Orthologs: mouse
Gene size: 85938bp
Exon count: 9