Atlas of Genetics and Cytogenetics in Oncology and Haematology


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SYNM (synemin)

Identity

Alias_namesDMN
desmuslin
synemin, intermediate filament protein
Alias_symbol (synonym)KIAA0353
SYN
Other alias
HGNC (Hugo) SYNM
LocusID (NCBI) 23336
Atlas_Id 50031
Location 15q26.3  [Link to chromosome band 15q26]
Location_base_pair Starts at 99645286 and ends at 99675800 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
SYNM (15q26.3) / KIF5B (10p11.22)

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)SYNM   24466
LRG (Locus Reference Genomic)LRG_415
Cards
Entrez_Gene (NCBI)SYNM  23336  synemin
AliasesDMN; SYN
GeneCards (Weizmann)SYNM
Ensembl hg19 (Hinxton)ENSG00000182253 [Gene_View]  chr15:99645286-99675800 [Contig_View]  SYNM [Vega]
Ensembl hg38 (Hinxton)ENSG00000182253 [Gene_View]  chr15:99645286-99675800 [Contig_View]  SYNM [Vega]
ICGC DataPortalENSG00000182253
TCGA cBioPortalSYNM
AceView (NCBI)SYNM
Genatlas (Paris)SYNM
WikiGenes23336
SOURCE (Princeton)SYNM
Genetics Home Reference (NIH)SYNM
Genomic and cartography
GoldenPath hg19 (UCSC)SYNM  -     chr15:99645286-99675800 +  15q26.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)SYNM  -     15q26.3   [Description]    (hg38-Dec_2013)
EnsemblSYNM - 15q26.3 [CytoView hg19]  SYNM - 15q26.3 [CytoView hg38]
Mapping of homologs : NCBISYNM [Mapview hg19]  SYNM [Mapview hg38]
OMIM606087   
Gene and transcription
Genbank (Entrez)AB002351 AF359284 AJ310521 AJ310522 AJ697971
RefSeq transcript (Entrez)NM_015286 NM_145728
RefSeq genomic (Entrez)NC_000015 NC_018926 NG_008210 NT_010194 NW_004929399
Consensus coding sequences : CCDS (NCBI)SYNM
Cluster EST : UnigeneHs.207106 [ NCBI ]
CGAP (NCI)Hs.207106
Alternative Splicing GalleryENSG00000182253
Gene ExpressionSYNM [ NCBI-GEO ]   SYNM [ EBI - ARRAY_EXPRESS ]   SYNM [ SEEK ]   SYNM [ MEM ]
Gene Expression Viewer (FireBrowse)SYNM [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)23336
GTEX Portal (Tissue expression)SYNM
Protein : pattern, domain, 3D structure
UniProt/SwissProtO15061   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO15061  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO15061
Splice isoforms : SwissVarO15061
PhosPhoSitePlusO15061
Domaine pattern : Prosite (Expaxy)IF (PS00226)   
Domains : Interpro (EBI)IF    Intermediate_filament_CS    SYNM   
Domain families : Pfam (Sanger)Filament (PF00038)   
Domain families : Pfam (NCBI)pfam00038   
Conserved Domain (NCBI)SYNM
DMDM Disease mutations23336
Blocks (Seattle)SYNM
SuperfamilyO15061
Human Protein AtlasENSG00000182253
Peptide AtlasO15061
HPRD07305
IPIIPI00299301   IPI00299302   IPI00921956   
Protein Interaction databases
DIP (DOE-UCLA)O15061
IntAct (EBI)O15061
FunCoupENSG00000182253
BioGRIDSYNM
STRING (EMBL)SYNM
ZODIACSYNM
Ontologies - Pathways
QuickGOO15061
Ontology : AmiGOstructural constituent of cytoskeleton  protein binding  intermediate filament  intermediate filament  adherens junction  structural constituent of muscle  membrane  vinculin binding  intermediate filament binding  costamere  intermediate filament cytoskeleton organization  neurofilament cytoskeleton  
Ontology : EGO-EBIstructural constituent of cytoskeleton  protein binding  intermediate filament  intermediate filament  adherens junction  structural constituent of muscle  membrane  vinculin binding  intermediate filament binding  costamere  intermediate filament cytoskeleton organization  neurofilament cytoskeleton  
NDEx NetworkSYNM
Atlas of Cancer Signalling NetworkSYNM
Wikipedia pathwaysSYNM
Orthology - Evolution
OrthoDB23336
GeneTree (enSembl)ENSG00000182253
Phylogenetic Trees/Animal Genes : TreeFamSYNM
HOVERGENO15061
HOGENOMO15061
Homologs : HomoloGeneSYNM
Homology/Alignments : Family Browser (UCSC)SYNM
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerSYNM [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)SYNM
dbVarSYNM
ClinVarSYNM
1000_GenomesSYNM 
Exome Variant ServerSYNM
ExAC (Exome Aggregation Consortium)SYNM (select the gene name)
Genetic variants : HAPMAP23336
Genomic Variants (DGV)SYNM [DGVbeta]
DECIPHER (Syndromes)15:99645286-99675800  ENSG00000182253
CONAN: Copy Number AnalysisSYNM 
Mutations
ICGC Data PortalSYNM 
TCGA Data PortalSYNM 
Broad Tumor PortalSYNM
OASIS PortalSYNM [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICSYNM  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDSYNM
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
BioMutasearch SYNM
DgiDB (Drug Gene Interaction Database)SYNM
DoCM (Curated mutations)SYNM (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)SYNM (select a term)
intoGenSYNM
Cancer3DSYNM(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM606087   
Orphanet
MedgenSYNM
Genetic Testing Registry SYNM
NextProtO15061 [Medical]
TSGene23336
GENETestsSYNM
Huge Navigator SYNM [HugePedia]
snp3D : Map Gene to Disease23336
BioCentury BCIQSYNM
ClinGenSYNM
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD23336
Chemical/Pharm GKB GenePA164726408
Clinical trialSYNM
Miscellaneous
canSAR (ICR)SYNM (select the gene name)
Probes
Litterature
PubMed35 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineSYNM
EVEXSYNM
GoPubMedSYNM
iHOPSYNM
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 13:30:04 CET 2017

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