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EVPLL (envoplakin like)

Identity

Other alias-
HGNC (Hugo) EVPLL
LocusID (NCBI) 645027
Atlas_Id 62937
Location 17p11.2  [Link to chromosome band 17p11]
Location_base_pair Starts at 18377765 and ends at 18389646 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)EVPLL   35236
Cards
Entrez_Gene (NCBI)EVPLL  645027  envoplakin like
Aliases
GeneCards (Weizmann)EVPLL
Ensembl hg19 (Hinxton)ENSG00000214860 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000214860 [Gene_View]  chr17:18377765-18389646 [Contig_View]  EVPLL [Vega]
ICGC DataPortalENSG00000214860
TCGA cBioPortalEVPLL
AceView (NCBI)EVPLL
Genatlas (Paris)EVPLL
WikiGenes645027
SOURCE (Princeton)EVPLL
Genetics Home Reference (NIH)EVPLL
Genomic and cartography
GoldenPath hg38 (UCSC)EVPLL  -     chr17:18377765-18389646 +  17p11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)EVPLL  -     17p11.2   [Description]    (hg19-Feb_2009)
EnsemblEVPLL - 17p11.2 [CytoView hg19]  EVPLL - 17p11.2 [CytoView hg38]
Mapping of homologs : NCBIEVPLL [Mapview hg19]  EVPLL [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK298286 BC026998 BC036791
RefSeq transcript (Entrez)NM_001145127
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)EVPLL
Cluster EST : UnigeneHs.462400 [ NCBI ]
CGAP (NCI)Hs.462400
Alternative Splicing GalleryENSG00000214860
Gene ExpressionEVPLL [ NCBI-GEO ]   EVPLL [ EBI - ARRAY_EXPRESS ]   EVPLL [ SEEK ]   EVPLL [ MEM ]
Gene Expression Viewer (FireBrowse)EVPLL [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)645027
GTEX Portal (Tissue expression)EVPLL
Human Protein AtlasENSG00000214860-EVPLL [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtA8MZ36   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA8MZ36  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA8MZ36
Splice isoforms : SwissVarA8MZ36
PhosPhoSitePlusA8MZ36
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)EVPLL
DMDM Disease mutations645027
Blocks (Seattle)EVPLL
SuperfamilyA8MZ36
Human Protein Atlas [tissue]ENSG00000214860-EVPLL [tissue]
Peptide AtlasA8MZ36
IPIIPI00745112   
Protein Interaction databases
DIP (DOE-UCLA)A8MZ36
IntAct (EBI)A8MZ36
FunCoupENSG00000214860
BioGRIDEVPLL
STRING (EMBL)EVPLL
ZODIACEVPLL
Ontologies - Pathways
QuickGOA8MZ36
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkEVPLL
Atlas of Cancer Signalling NetworkEVPLL
Wikipedia pathwaysEVPLL
Orthology - Evolution
OrthoDB645027
GeneTree (enSembl)ENSG00000214860
Phylogenetic Trees/Animal Genes : TreeFamEVPLL
HOVERGENA8MZ36
HOGENOMA8MZ36
Homologs : HomoloGeneEVPLL
Homology/Alignments : Family Browser (UCSC)EVPLL
Gene fusions - Rearrangements
Tumor Fusion PortalEVPLL
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerEVPLL [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)EVPLL
dbVarEVPLL
ClinVarEVPLL
1000_GenomesEVPLL 
Exome Variant ServerEVPLL
ExAC (Exome Aggregation Consortium)ENSG00000214860
GNOMAD BrowserENSG00000214860
Genetic variants : HAPMAP645027
Genomic Variants (DGV)EVPLL [DGVbeta]
DECIPHEREVPLL [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisEVPLL 
Mutations
ICGC Data PortalEVPLL 
TCGA Data PortalEVPLL 
Broad Tumor PortalEVPLL
OASIS PortalEVPLL [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICEVPLL  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDEVPLL
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch EVPLL
DgiDB (Drug Gene Interaction Database)EVPLL
DoCM (Curated mutations)EVPLL (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)EVPLL (select a term)
intoGenEVPLL
Cancer3DEVPLL(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETEVPLL
MedgenEVPLL
Genetic Testing Registry EVPLL
NextProtA8MZ36 [Medical]
TSGene645027
GENETestsEVPLL
Target ValidationEVPLL
Huge Navigator EVPLL [HugePedia]
snp3D : Map Gene to Disease645027
BioCentury BCIQEVPLL
ClinGenEVPLL
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD645027
Chemical/Pharm GKB GenePA164719396
Clinical trialEVPLL
Miscellaneous
canSAR (ICR)EVPLL (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineEVPLL
EVEXEVPLL
GoPubMedEVPLL
iHOPEVPLL
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Nov 20 19:28:06 CET 2017

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