Bos taurus Gene: WASF2
Summary
InnateDB Gene IDBG-645020.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol WASF2
Gene Name Wiskott-Aldrich syndrome protein family member 2
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000018374
Encoded Proteins
Wiskott-Aldrich syndrome protein family member 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000158195:
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]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:126399312-126469335
Strand Forward strand
Band
Transcripts
ENSBTAT00000024447 ENSBTAP00000024447
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 19 interaction(s) predicted by orthology.
Predicted by orthology
Total 19 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003779 actin binding
GO:0005515 protein binding
GO:0032403 protein complex binding
Biological Process
GO:0001525 angiogenesis
GO:0001667 ameboidal cell migration
GO:0006897 endocytosis
GO:0006928 cellular component movement
GO:0010592 positive regulation of lamellipodium assembly
GO:0016601 Rac protein signal transduction
GO:0030032 lamellipodium assembly
GO:0030036 actin cytoskeleton organization
GO:0030048 actin filament-based movement
GO:0035855 megakaryocyte development
GO:0051497 negative regulation of stress fiber assembly
GO:0072673 lamellipodium morphogenesis
Cellular Component
GO:0001726 ruffle
GO:0005622 intracellular
GO:0005737 cytoplasm
GO:0005769 early endosome
GO:0005856 cytoskeleton
GO:0005911 cell-cell junction
GO:0030027 lamellipodium
GO:0031209 SCAR complex
GO:0042995 cell projection
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathways
NETPATH
REACTOME
Fcgamma receptor (FCGR) dependent phagocytosis pathway
VEGFA-VEGFR2 Pathway pathway
Immune System pathway
Signal Transduction pathway
Regulation of actin dynamics for phagocytic cup formation pathway
Signaling by VEGF pathway
Innate Immune System pathway
KEGG
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
TCR pathway
REACTOME
Regulation of actin dynamics for phagocytic cup formation pathway
Signaling by VEGF pathway
Innate Immune System pathway
Signal Transduction pathway
Immune System pathway
VEGFA-VEGFR2 Pathway pathway
Fcgamma receptor (FCGR) dependent phagocytosis pathway
Innate Immune System pathway
Regulation of actin dynamics for phagocytic cup formation pathway
Signaling by VEGF pathway
Immune System pathway
VEGFA-VEGFR2 Pathway pathway
Fcgamma receptor (FCGR) dependent phagocytosis pathway
Signal Transduction pathway
KEGG
Regulation of actin cytoskeleton pathway
Adherens junction pathway
Fc gamma R-mediated phagocytosis pathway
Bacterial invasion of epithelial cells pathway
Shigellosis pathway
Regulation of actin cytoskeleton pathway
Adherens junction pathway
Fc gamma R-mediated phagocytosis pathway
Bacterial invasion of epithelial cells pathway
INOH
PID NCI
E-cadherin signaling in the nascent adherens junction
ErbB1 downstream signaling
RAC1 signaling pathway
PDGFR-beta signaling pathway
Cross-References
SwissProt A2VDK6
TrEMBL
UniProt Splice Variant
Entrez Gene 504482
UniGene Bt.38300
RefSeq NM_001081511 XM_005203087 XM_005203088
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BC133284
GenPept AAI33285
RNA Seq Atlas 504482