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EPWW6493 (uncharacterized LOC100129831)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100129831
Atlas_Id 62875
Location 19p13.3  [Link to chromosome band 19p13]
Location_base_pair Starts at 2294607 and ends at 2295571 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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)EPWW6493  100129831  uncharacterized LOC100129831
Aliases
GeneCards (Weizmann)EPWW6493
Ensembl hg19 (Hinxton) [Gene_View]  chr19:2294607-2295571 [Contig_View]  EPWW6493 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr19:2294607-2295571 [Contig_View]  EPWW6493 [Vega]
TCGA cBioPortalEPWW6493
AceView (NCBI)EPWW6493
Genatlas (Paris)EPWW6493
WikiGenes100129831
SOURCE (Princeton)EPWW6493
Genetics Home Reference (NIH)EPWW6493
Genomic and cartography
GoldenPath hg19 (UCSC)EPWW6493  -     chr19:2294607-2295571 +  19p13.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)EPWW6493  -     19p13.3   [Description]    (hg38-Dec_2013)
EnsemblEPWW6493 - 19p13.3 [CytoView hg19]  EPWW6493 - 19p13.3 [CytoView hg38]
Mapping of homologs : NCBIEPWW6493 [Mapview hg19]  EPWW6493 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AY358234
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)AC_000151 NC_000019 NC_018930 NT_011255 NW_001838476 NW_004078096
Consensus coding sequences : CCDS (NCBI)EPWW6493
Cluster EST : UnigeneHs.635444 [ NCBI ]
CGAP (NCI)Hs.635444
Gene ExpressionEPWW6493 [ NCBI-GEO ]   EPWW6493 [ EBI - ARRAY_EXPRESS ]   EPWW6493 [ SEEK ]   EPWW6493 [ MEM ]
Gene Expression Viewer (FireBrowse)EPWW6493 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100129831
GTEX Portal (Tissue expression)EPWW6493
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6UXR8   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6UXR8  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6UXR8
Splice isoforms : SwissVarQ6UXR8
PhosPhoSitePlusQ6UXR8
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)EPWW6493
DMDM Disease mutations100129831
Blocks (Seattle)EPWW6493
SuperfamilyQ6UXR8
Peptide AtlasQ6UXR8
IPIIPI00432694   
Protein Interaction databases
DIP (DOE-UCLA)Q6UXR8
IntAct (EBI)Q6UXR8
BioGRIDEPWW6493
STRING (EMBL)EPWW6493
ZODIACEPWW6493
Ontologies - Pathways
QuickGOQ6UXR8
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkEPWW6493
Atlas of Cancer Signalling NetworkEPWW6493
Wikipedia pathwaysEPWW6493
Orthology - Evolution
OrthoDB100129831
Phylogenetic Trees/Animal Genes : TreeFam-
HOVERGENQ6UXR8
HOGENOMQ6UXR8
Homologs : HomoloGeneEPWW6493
Homology/Alignments : Family Browser (UCSC)EPWW6493
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerEPWW6493 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)EPWW6493
dbVarEPWW6493
ClinVarEPWW6493
1000_GenomesEPWW6493 
Exome Variant ServerEPWW6493
ExAC (Exome Aggregation Consortium)EPWW6493 (select the gene name)
Genetic variants : HAPMAP100129831
Genomic Variants (DGV)EPWW6493 [DGVbeta]
DECIPHER (Syndromes)19:2294607-2295571  
CONAN: Copy Number AnalysisEPWW6493 
Mutations
ICGC Data Portal- 
TCGA Data Portal- 
Broad Tumor Portal-
OASIS Portal- [ Somatic mutations - Copy number]
Mutations and Diseases : HGMD-
BioMutasearch EPWW6493
DgiDB (Drug Gene Interaction Database)EPWW6493
DoCM (Curated mutations)EPWW6493 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)EPWW6493 (select a term)
intoGenEPWW6493
Cancer3DEPWW6493(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenEPWW6493
Genetic Testing Registry EPWW6493
NextProtQ6UXR8 [Medical]
TSGene100129831
GENETestsEPWW6493
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100129831
BioCentury BCIQEPWW6493
ClinGenEPWW6493
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100129831
Clinical trialEPWW6493
Miscellaneous
canSAR (ICR)EPWW6493 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineEPWW6493
EVEXEPWW6493
GoPubMedEPWW6493
iHOPEPWW6493
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 : Tue Mar 14 12:03:01 CET 2017

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