Atlas of Genetics and Cytogenetics in Oncology and Haematology


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ERAS (ES cell expressed Ras)

Identity

Alias_namesHRAS2
HRASP
v-Ha-ras Harvey rat sarcoma viral oncogene homolog pseudogene
Other alias
HGNC (Hugo) ERAS
LocusID (NCBI) 3266
Atlas_Id 43246
Location Xp11.23  [Link to chromosome band Xp11]
Location_base_pair Starts at 48826513 and ends at 48829869 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)ERAS   5174
Cards
Entrez_Gene (NCBI)ERAS  3266  ES cell expressed Ras
AliasesHRAS2; HRASP
GeneCards (Weizmann)ERAS
Ensembl hg19 (Hinxton)ENSG00000187682 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000187682 [Gene_View]  chrX:48826513-48829869 [Contig_View]  ERAS [Vega]
ICGC DataPortalENSG00000187682
TCGA cBioPortalERAS
AceView (NCBI)ERAS
Genatlas (Paris)ERAS
WikiGenes3266
SOURCE (Princeton)ERAS
Genetics Home Reference (NIH)ERAS
Genomic and cartography
GoldenPath hg38 (UCSC)ERAS  -     chrX:48826513-48829869 +  Xp11.23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ERAS  -     Xp11.23   [Description]    (hg19-Feb_2009)
EnsemblERAS - Xp11.23 [CytoView hg19]  ERAS - Xp11.23 [CytoView hg38]
Mapping of homologs : NCBIERAS [Mapview hg19]  ERAS [Mapview hg38]
OMIM300437   
Gene and transcription
Genbank (Entrez)AB093575 BC101642 BC101644 HY043532
RefSeq transcript (Entrez)NM_181532
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ERAS
Cluster EST : UnigeneHs.447330 [ NCBI ]
CGAP (NCI)Hs.447330
Alternative Splicing GalleryENSG00000187682
Gene ExpressionERAS [ NCBI-GEO ]   ERAS [ EBI - ARRAY_EXPRESS ]   ERAS [ SEEK ]   ERAS [ MEM ]
Gene Expression Viewer (FireBrowse)ERAS [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)3266
GTEX Portal (Tissue expression)ERAS
Human Protein AtlasENSG00000187682-ERAS [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ7Z444   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ7Z444  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ7Z444
Splice isoforms : SwissVarQ7Z444
PhosPhoSitePlusQ7Z444
Domaine pattern : Prosite (Expaxy)RAS (PS51421)   
Domains : Interpro (EBI)P-loop_NTPase    Small_GTP-bd_dom    Small_GTPase    Small_GTPase_Ras   
Domain families : Pfam (Sanger)Ras (PF00071)   
Domain families : Pfam (NCBI)pfam00071   
Conserved Domain (NCBI)ERAS
DMDM Disease mutations3266
Blocks (Seattle)ERAS
SuperfamilyQ7Z444
Human Protein Atlas [tissue]ENSG00000187682-ERAS [tissue]
Peptide AtlasQ7Z444
HPRD02339
IPIIPI00375882   
Protein Interaction databases
DIP (DOE-UCLA)Q7Z444
IntAct (EBI)Q7Z444
FunCoupENSG00000187682
BioGRIDERAS
STRING (EMBL)ERAS
ZODIACERAS
Ontologies - Pathways
QuickGOQ7Z444
Ontology : AmiGOGTPase activity  GTP binding  plasma membrane  signal transduction  
Ontology : EGO-EBIGTPase activity  GTP binding  plasma membrane  signal transduction  
NDEx NetworkERAS
Atlas of Cancer Signalling NetworkERAS
Wikipedia pathwaysERAS
Orthology - Evolution
OrthoDB3266
GeneTree (enSembl)ENSG00000187682
Phylogenetic Trees/Animal Genes : TreeFamERAS
HOVERGENQ7Z444
HOGENOMQ7Z444
Homologs : HomoloGeneERAS
Homology/Alignments : Family Browser (UCSC)ERAS
Gene fusions - Rearrangements
Tumor Fusion PortalERAS
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerERAS [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ERAS
dbVarERAS
ClinVarERAS
1000_GenomesERAS 
Exome Variant ServerERAS
ExAC (Exome Aggregation Consortium)ENSG00000187682
GNOMAD BrowserENSG00000187682
Genetic variants : HAPMAP3266
Genomic Variants (DGV)ERAS [DGVbeta]
DECIPHERERAS [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisERAS 
Mutations
ICGC Data PortalERAS 
TCGA Data PortalERAS 
Broad Tumor PortalERAS
OASIS PortalERAS [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICERAS  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDERAS
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch ERAS
DgiDB (Drug Gene Interaction Database)ERAS
DoCM (Curated mutations)ERAS (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ERAS (select a term)
intoGenERAS
Cancer3DERAS(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM300437   
Orphanet
DisGeNETERAS
MedgenERAS
Genetic Testing Registry ERAS
NextProtQ7Z444 [Medical]
TSGene3266
GENETestsERAS
Target ValidationERAS
Huge Navigator ERAS [HugePedia]
snp3D : Map Gene to Disease3266
BioCentury BCIQERAS
ClinGenERAS
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD3266
Chemical/Pharm GKB GenePA29448
Clinical trialERAS
Miscellaneous
canSAR (ICR)ERAS (select the gene name)
Probes
Litterature
PubMed22 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineERAS
EVEXERAS
GoPubMedERAS
iHOPERAS
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Nov 21 14:12:13 CET 2017

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