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ESRG (embryonic stem cell related (non-protein coding))

Identity

Alias_symbol (synonym)HESRG
Other alias
HGNC (Hugo) ESRG
LocusID (NCBI) 790952
Atlas_Id 52668
Location 3p14.3  [Link to chromosome band 3p14]
Location_base_pair Starts at 54666151 and ends at 54673884 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)ESRG   39079
Cards
Entrez_Gene (NCBI)ESRG  790952  embryonic stem cell related (non-protein coding)
AliasesHESRG
GeneCards (Weizmann)ESRG
Ensembl hg19 (Hinxton)ENSG00000265992 [Gene_View]  chr3:54666151-54673884 [Contig_View]  ESRG [Vega]
Ensembl hg38 (Hinxton)ENSG00000265992 [Gene_View]  chr3:54666151-54673884 [Contig_View]  ESRG [Vega]
ICGC DataPortalENSG00000265992
TCGA cBioPortalESRG
AceView (NCBI)ESRG
Genatlas (Paris)ESRG
WikiGenes790952
SOURCE (Princeton)ESRG
Genetics Home Reference (NIH)ESRG
Genomic and cartography
GoldenPath hg19 (UCSC)ESRG  -     chr3:54666151-54673884 -  3p14.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)ESRG  -     3p14.3   [Description]    (hg38-Dec_2013)
EnsemblESRG - 3p14.3 [CytoView hg19]  ESRG - 3p14.3 [CytoView hg38]
Mapping of homologs : NCBIESRG [Mapview hg19]  ESRG [Mapview hg38]
OMIM611473   
Gene and transcription
Genbank (Entrez)BE672034 DQ445779 HG495687 KM363598
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000003 NC_018914 NT_022517 NW_004929309
Consensus coding sequences : CCDS (NCBI)ESRG
Cluster EST : UnigeneHs.720658 [ NCBI ]
CGAP (NCI)Hs.720658
Alternative Splicing GalleryENSG00000265992
Gene ExpressionESRG [ NCBI-GEO ]   ESRG [ EBI - ARRAY_EXPRESS ]   ESRG [ SEEK ]   ESRG [ MEM ]
Gene Expression Viewer (FireBrowse)ESRG [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)790952
GTEX Portal (Tissue expression)ESRG
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ1W209   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ1W209  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ1W209
Splice isoforms : SwissVarQ1W209
PhosPhoSitePlusQ1W209
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)ESRG
DMDM Disease mutations790952
Blocks (Seattle)ESRG
SuperfamilyQ1W209
Human Protein AtlasENSG00000265992
Peptide AtlasQ1W209
IPIIPI00745377   
Protein Interaction databases
DIP (DOE-UCLA)Q1W209
IntAct (EBI)Q1W209
FunCoupENSG00000265992
BioGRIDESRG
STRING (EMBL)ESRG
ZODIACESRG
Ontologies - Pathways
QuickGOQ1W209
Ontology : AmiGOnucleus  
Ontology : EGO-EBInucleus  
NDEx NetworkESRG
Atlas of Cancer Signalling NetworkESRG
Wikipedia pathwaysESRG
Orthology - Evolution
OrthoDB790952
GeneTree (enSembl)ENSG00000265992
Phylogenetic Trees/Animal Genes : TreeFamESRG
HOVERGENQ1W209
HOGENOMQ1W209
Homologs : HomoloGeneESRG
Homology/Alignments : Family Browser (UCSC)ESRG
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerESRG [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ESRG
dbVarESRG
ClinVarESRG
1000_GenomesESRG 
Exome Variant ServerESRG
ExAC (Exome Aggregation Consortium)ESRG (select the gene name)
Genetic variants : HAPMAP790952
Genomic Variants (DGV)ESRG [DGVbeta]
DECIPHER (Syndromes)3:54666151-54673884  ENSG00000265992
CONAN: Copy Number AnalysisESRG 
Mutations
ICGC Data PortalESRG 
TCGA Data PortalESRG 
Broad Tumor PortalESRG
OASIS PortalESRG [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDESRG
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ESRG
DgiDB (Drug Gene Interaction Database)ESRG
DoCM (Curated mutations)ESRG (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ESRG (select a term)
intoGenESRG
Cancer3DESRG(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM611473   
Orphanet
MedgenESRG
Genetic Testing Registry ESRG
NextProtQ1W209 [Medical]
TSGene790952
GENETestsESRG
Huge Navigator ESRG [HugePedia]
snp3D : Map Gene to Disease790952
BioCentury BCIQESRG
ClinGenESRG
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD790952
Clinical trialESRG
Miscellaneous
canSAR (ICR)ESRG (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineESRG
EVEXESRG
GoPubMedESRG
iHOPESRG
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Mar 30 15:00:22 CEST 2017

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