WASF2

WASF2
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesWASF2, IMD2, SCAR2, WASF4, WAVE2, dJ393P12.2, WAS protein family member 2, WASP family member 2
External IDsOMIM: 605875; MGI: 1098641; HomoloGene: 86743; GeneCards: WASF2; OMA:WASF2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

10163

242687

Ensembl

ENSG00000158195

ENSMUSG00000028868

UniProt

Q9Y6W5

Q8BH43

RefSeq (mRNA)

NM_006990
NM_001201404

NM_153423

RefSeq (protein)

NP_001188333
NP_008921

NP_700472

Location (UCSC)Chr 1: 27.4 – 27.49 MbChr 4: 132.86 – 132.93 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Wiskott–Aldrich syndrome protein family member 2 is a protein that in humans is encoded by the WASF2 gene.

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 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.