Mus musculus Gene: Gsn
Summary
InnateDB Gene IDBG-164316.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Gsn
Gene Name gelsolin
Synonyms
Species Mus musculus
Ensembl Gene ENSMUSG00000026879
Encoded Proteins
gelsolin
gelsolin
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 ENSG00000148180:
The protein encoded by this gene binds to the "plus" ends of actin monomers and filaments to prevent monomer exchange. The encoded calcium-regulated protein functions in both assembly and disassembly of actin filaments. Defects in this gene are a cause of familial amyloidosis Finnish type (FAF). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
The protein encoded by this gene binds to the "plus" ends of actin monomers and filaments to prevent monomer exchange. The encoded calcium-regulated protein functions in both assembly and disassembly of actin filaments. Defects in this gene are a cause of familial amyloidosis Finnish type (FAF). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:35279663-35307892
Strand Forward strand
Band B
Transcripts
ENSMUST00000028239 ENSMUSP00000028239
ENSMUST00000142324 ENSMUSP00000118120
ENSMUST00000124323
ENSMUST00000139867
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 17 experimentally validated interaction(s) in this database.
They are also associated with 30 interaction(s) predicted by orthology.
Experimentally validated
Total 17 [view]
Protein-Protein 17 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 30 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003779 actin binding
GO:0005515 protein binding
GO:0046872 metal ion binding
Biological Process
GO:0006915 apoptotic process
GO:0007568 aging
GO:0008154 actin polymerization or depolymerization
GO:0014003 oligodendrocyte development
GO:0016192 vesicle-mediated transport
GO:0030041 actin filament polymerization
GO:0030155 regulation of cell adhesion
GO:0042060 wound healing
GO:0042246 tissue regeneration
GO:0045471 response to ethanol
GO:0048015 phosphatidylinositol-mediated signaling
GO:0051014 actin filament severing
GO:0051593 response to folic acid
GO:0051693 actin filament capping
GO:0060271 cilium morphogenesis
GO:0071276 cellular response to cadmium ion
Cellular Component
GO:0001726 ruffle
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005829 cytosol
GO:0015629 actin cytoskeleton
GO:0030027 lamellipodium
GO:0043234 protein complex
GO:0048471 perinuclear region of cytoplasm
GO:0070062 extracellular vesicular exosome
GO:0072562 blood microparticle
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
Apoptosis pathway
Disease pathway
Amyloids pathway
Apoptotic cleavage of cellular proteins pathway
Caspase-mediated cleavage of cytoskeletal proteins pathway
Apoptotic execution phase pathway
KEGG
Regulation of actin cytoskeleton pathway
Fc gamma R-mediated phagocytosis pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
AndrogenReceptor pathway
EGFR1 pathway
REACTOME
Caspase-mediated cleavage of cytoskeletal proteins pathway
Apoptotic cleavage of cellular proteins pathway
Apoptotic execution phase pathway
Amyloids pathway
Apoptosis pathway
Disease pathway
KEGG
Regulation of actin cytoskeleton pathway
Fc gamma R-mediated phagocytosis pathway
INOH
PID NCI
Caspase Cascade in Apoptosis
Coregulation of Androgen receptor activity
N-cadherin signaling events
Osteopontin-mediated events
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.21109 Mm.470521
RefSeq NM_001206367 NM_001206368 NM_001206369 NM_146120 XM_006497990 XM_006497991 XM_006497992 XM_006497993
OMIM
CCDS CCDS15960
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas