Atlas of Genetics and Cytogenetics in Oncology and Haematology


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GSN (gelsolin)

Identity

Other namesADF
AGEL
HGNC (Hugo) GSN
LocusID (NCBI) 2934
Location 9q33.2
Location_base_pair Starts at 124062079 and ends at 124095120 bp from pter ( according to hg19-Feb_2009)
Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 

External links

Nomenclature
HGNC (Hugo)GSN   4620
Cards
Entrez_Gene (NCBI)GSN  2934  gelsolin
GeneCards (Weizmann)GSN
Ensembl (Hinxton)ENSG00000148180 [Gene_View]  chr9:124062079-124095120 [Contig_View]  GSN [Vega]
ICGC DataPortalENSG00000148180
AceView (NCBI)GSN
Genatlas (Paris)GSN
WikiGenes2934
SOURCE (Princeton)NM_000177 NM_001127662 NM_001127663 NM_001127664 NM_001127665 NM_001127666 NM_001127667 NM_001258029 NM_001258030 NM_198252
Genomic and cartography
GoldenPath (UCSC)GSN  -  9q33.2   chr9:124062079-124095120 +  9q33.2   [Description]    (hg19-Feb_2009)
EnsemblGSN - 9q33.2 [CytoView]
Mapping of homologs : NCBIGSN [Mapview]
OMIM105120   137350   
Gene and transcription
Genbank (Entrez)AI742454 AK092797 AK096280 AK125819 AK295201
RefSeq transcript (Entrez)NM_000177 NM_001127662 NM_001127663 NM_001127664 NM_001127665 NM_001127666 NM_001127667 NM_001258029 NM_001258030 NM_198252
RefSeq genomic (Entrez)AC_000141 NC_000009 NC_018920 NG_012872 NT_008470 NW_001839237 NW_004929366
Consensus coding sequences : CCDS (NCBI)GSN
Cluster EST : UnigeneHs.522373 [ NCBI ]
CGAP (NCI)Hs.522373
Alternative Splicing : Fast-db (Paris)GSHG0030419
Alternative Splicing GalleryENSG00000148180
Gene ExpressionGSN [ NCBI-GEO ]     GSN [ SEEK ]   GSN [ MEM ]
Protein : pattern, domain, 3D structure
UniProt/SwissProtP06396 (Uniprot)
NextProtP06396  [Medical]
With graphics : InterProP06396
Splice isoforms : SwissVarP06396 (Swissvar)
Domains : Interpro (EBI)ADF-H/Gelsolin-like_dom    Gelsolin-like_dom    Villin/Gelsolin   
Related proteins : CluSTrP06396
Domain families : Pfam (Sanger)Gelsolin (PF00626)   
Domain families : Pfam (NCBI)pfam00626   
Domain families : Smart (EMBL)GEL (SM00262)  
DMDM Disease mutations2934
Blocks (Seattle)P06396
PDB (SRS)1C0F    1C0G    1D4X    1DEJ    1EQY    1ESV    1H1V    1KCQ    1MDU    1NLV    1NM1    1NMD    1P8X    1P8Z    1SOL    1T44    1YAG    1YVN    2FF3    2FF6    2FH1    2FH2    2FH3    2FH4    3A5L    3A5M    3A5N    3A5O    3CI5    3CIP    3CJB    3CJC    3FFK    3FFN    3TU5   
PDB (PDBSum)1C0F    1C0G    1D4X    1DEJ    1EQY    1ESV    1H1V    1KCQ    1MDU    1NLV    1NM1    1NMD    1P8X    1P8Z    1SOL    1T44    1YAG    1YVN    2FF3    2FF6    2FH1    2FH2    2FH3    2FH4    3A5L    3A5M    3A5N    3A5O    3CI5    3CIP    3CJB    3CJC    3FFK    3FFN    3TU5   
PDB (IMB)1C0F    1C0G    1D4X    1DEJ    1EQY    1ESV    1H1V    1KCQ    1MDU    1NLV    1NM1    1NMD    1P8X    1P8Z    1SOL    1T44    1YAG    1YVN    2FF3    2FF6    2FH1    2FH2    2FH3    2FH4    3A5L    3A5M    3A5N    3A5O    3CI5    3CIP    3CJB    3CJC    3FFK    3FFN    3TU5   
PDB (RSDB)1C0F    1C0G    1D4X    1DEJ    1EQY    1ESV    1H1V    1KCQ    1MDU    1NLV    1NM1    1NMD    1P8X    1P8Z    1SOL    1T44    1YAG    1YVN    2FF3    2FF6    2FH1    2FH2    2FH3    2FH4    3A5L    3A5M    3A5N    3A5O    3CI5    3CIP    3CJB    3CJC    3FFK    3FFN    3TU5   
Human Protein AtlasENSG00000148180
Peptide AtlasP06396
HPRD00674
IPIIPI00026314   IPI00646773   IPI01009415   IPI00796316   IPI01015050   IPI00647556   IPI00641047   IPI00513782   IPI00377087   
Protein Interaction databases
DIP (DOE-UCLA)P06396
IntAct (EBI)P06396
FunCoupENSG00000148180
BioGRIDGSN
InParanoidP06396
Interologous Interaction database P06396
IntegromeDBGSN
STRING (EMBL)GSN
Ontologies - Pathways
Ontology : AmiGOruffle  actin binding  calcium ion binding  protein binding  extracellular region  extracellular region  extracellular region  extracellular region  cytosol  cytosol  cytosol  apoptotic process  cellular component disassembly involved in execution phase of apoptosis  aging  oligodendrocyte development  actin cytoskeleton  vesicle-mediated transport  lamellipodium  actin filament polymerization  actin filament polymerization  regulation of cell adhesion  tissue regeneration  protein complex  response to ethanol  phosphatidylinositol-mediated signaling  perinuclear region of cytoplasm  actin filament severing  actin filament severing  barbed-end actin filament capping  response to folic acid  cilium morphogenesis  extracellular vesicular exosome  cellular response to cadmium ion  blood microparticle  
Ontology : EGO-EBIruffle  actin binding  calcium ion binding  protein binding  extracellular region  extracellular region  extracellular region  extracellular region  cytosol  cytosol  cytosol  apoptotic process  cellular component disassembly involved in execution phase of apoptosis  aging  oligodendrocyte development  actin cytoskeleton  vesicle-mediated transport  lamellipodium  actin filament polymerization  actin filament polymerization  regulation of cell adhesion  tissue regeneration  protein complex  response to ethanol  phosphatidylinositol-mediated signaling  perinuclear region of cytoplasm  actin filament severing  actin filament severing  barbed-end actin filament capping  response to folic acid  cilium morphogenesis  extracellular vesicular exosome  cellular response to cadmium ion  blood microparticle  
Pathways : BIOCARTAErk and PI-3 Kinase Are Necessary for Collagen Binding in Corneal Epithelia [Genes]    Rho cell motility signaling pathway [Genes]    HIV-I Nef: negative effector of Fas and TNF [Genes]   
Pathways : KEGGFc gamma R-mediated phagocytosis    Regulation of actin cytoskeleton    Viral carcinogenesis   
Protein Interaction DatabaseGSN
Wikipedia pathwaysGSN
Gene fusion - rearrangments
Polymorphisms : SNP, mutations, diseases
SNP Single Nucleotide Polymorphism (NCBI)GSN
SNP (GeneSNP Utah)GSN
SNP : HGBaseGSN
Genetic variants : HAPMAPGSN
1000_GenomesGSN 
ICGC programENSG00000148180 
CONAN: Copy Number AnalysisGSN 
Somatic Mutations in Cancer : COSMICGSN 
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
Mutations and Diseases : HGMDGSN
OMIM105120    137350   
MedgenGSN
GENETestsGSN
Disease Genetic AssociationGSN
Huge Navigator GSN [HugePedia]  GSN [HugeCancerGEM]
Genomic VariantsGSN  GSN [DGVbeta]
Exome VariantGSN
dbVarGSN
ClinVarGSN
snp3D : Map Gene to Disease2934
General knowledge
Homologs : HomoloGeneGSN
Homology/Alignments : Family Browser (UCSC)GSN
Phylogenetic Trees/Animal Genes : TreeFamGSN
Chemical/Protein Interactions : CTD2934
Chemical/Pharm GKB GenePA29011
Clinical trialGSN
Cancer Resource (Charite)ENSG00000148180
Other databases
Probes
Litterature
PubMed167 Pubmed reference(s) in Entrez
CoreMineGSN
iHOPGSN
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

Contributor(s)

Written09-2002Dessen P, Le Minor S
Updated12-2013Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Oct 13 12:49:26 CEST 2014

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