WASF3

Identifiers

Aliases, Brush-1, SCAR3, WAVE3, WAS protein family member 3, WASP family member 3

External IDsOMIM: ; MGI: ; HomoloGene: ; GeneCards: ; OMA:

Gene location ( Human )

Chr.Chromosome 13 (human)

Band 13q12.13 Start 26,557,683 bp

End26,688,948 bp

Gene location ( Mouse )

Chr.Chromosome 5 (mouse)

Band 5|5 G3 Start 146,321,795 bp

End146,410,425 bp

RNA expression pattern

HumanMouse (ortholog)pars compacta pars reticulata paraflocculus of cerebellum lateral nuclear group of thalamus orbitofrontal cortex cerebellar vermis postcentral gyrus external globus pallidus Brodmann area 46 dorsal motor nucleus of vagus nerveventral tegmental area neural layer of retina lobe of cerebellum cerebellar vermis dorsomedial hypothalamic nucleus mammillary body globus pallidus lateral hypothalamus lateral septal nucleus deep cerebellar nuclei

Human Mouse (ortholog)

pars compacta pars reticulata paraflocculus of cerebellum lateral nuclear group of thalamus orbitofrontal cortex cerebellar vermis postcentral gyrus external globus pallidus Brodmann area 46 dorsal motor nucleus of vagus nerveventral tegmental area neural layer of retina lobe of cerebellum cerebellar vermis dorsomedial hypothalamic nucleus mammillary body globus pallidus lateral hypothalamus lateral septal nucleus deep cerebellar nuclei

ventral tegmental area neural layer of retina lobe of cerebellum cerebellar vermis dorsomedial hypothalamic nucleus mammillary body globus pallidus lateral hypothalamus lateral septal nucleus deep cerebellar nuclei

Gene ontologyMolecular functionCellular componentBiological processSources: /

Gene ontology

Molecular function

Cellular component

Biological process

Sources: /

OrthologsSpeciesHumanMouseEntrez Ensembl UniProtRefSeq (mRNA)RefSeq (protein)Location (UCSC)PubMed search

Orthologs

Species Human Mouse

Entrez

Ensembl

UniProt

RefSeq (mRNA)

RefSeq (protein)

Location (UCSC)

PubMed search

Wikidata

View/Edit HumanView/Edit Mouse

Wiskott–Aldrich syndrome protein family member 3 is a protein that in humans is encoded by the WASF3 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 transduce signals that involve changes in cell shape, motility or function.

WASF3

See also

Further reading