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ENO4 (enolase family member 4)

Identity

Alias_namesC10orf134
chromosome 10 open reading frame 134
Alias_symbol (synonym)AC023283.3
Other alias
HGNC (Hugo) ENO4
LocusID (NCBI) 387712
Atlas_Id 62835
Location 10q25.3  [Link to chromosome band 10q25]
Location_base_pair Starts at 116849512 and ends at 116882601 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)ENO4   31670
Cards
Entrez_Gene (NCBI)ENO4  387712  enolase family member 4
AliasesC10orf134
GeneCards (Weizmann)ENO4
Ensembl hg19 (Hinxton)ENSG00000188316 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000188316 [Gene_View]  chr10:116849512-116882601 [Contig_View]  ENO4 [Vega]
ICGC DataPortalENSG00000188316
TCGA cBioPortalENO4
AceView (NCBI)ENO4
Genatlas (Paris)ENO4
WikiGenes387712
SOURCE (Princeton)ENO4
Genetics Home Reference (NIH)ENO4
Genomic and cartography
GoldenPath hg38 (UCSC)ENO4  -     chr10:116849512-116882601 +  10q25.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)ENO4  -     10q25.3   [Description]    (hg19-Feb_2009)
EnsemblENO4 - 10q25.3 [CytoView hg19]  ENO4 - 10q25.3 [CytoView hg38]
Mapping of homologs : NCBIENO4 [Mapview hg19]  ENO4 [Mapview hg38]
OMIM131375   
Gene and transcription
Genbank (Entrez)BX647301
RefSeq transcript (Entrez)NM_001242699
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)ENO4
Cluster EST : UnigeneHs.693248 [ NCBI ]
CGAP (NCI)Hs.693248
Alternative Splicing GalleryENSG00000188316
Gene ExpressionENO4 [ NCBI-GEO ]   ENO4 [ EBI - ARRAY_EXPRESS ]   ENO4 [ SEEK ]   ENO4 [ MEM ]
Gene Expression Viewer (FireBrowse)ENO4 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)387712
GTEX Portal (Tissue expression)ENO4
Human Protein AtlasENSG00000188316-ENO4 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtA6NNW6   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtA6NNW6  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProA6NNW6
Splice isoforms : SwissVarA6NNW6
Catalytic activity : Enzyme4.2.1.11 [ Enzyme-Expasy ]   4.2.1.114.2.1.11 [ IntEnz-EBI ]   4.2.1.11 [ BRENDA ]   4.2.1.11 [ KEGG ]   
PhosPhoSitePlusA6NNW6
Domains : Interpro (EBI)Enolase    Enolase_C    Enolase_C-like    Enolase_N    Enolase_N-like   
Domain families : Pfam (Sanger)Enolase_C (PF00113)    Enolase_N (PF03952)   
Domain families : Pfam (NCBI)pfam00113    pfam03952   
Domain families : Smart (EMBL)Enolase_C (SM01192)  Enolase_N (SM01193)  
Conserved Domain (NCBI)ENO4
DMDM Disease mutations387712
Blocks (Seattle)ENO4
SuperfamilyA6NNW6
Human Protein Atlas [tissue]ENSG00000188316-ENO4 [tissue]
Peptide AtlasA6NNW6
IPIIPI00888542   IPI00953311   
Protein Interaction databases
DIP (DOE-UCLA)A6NNW6
IntAct (EBI)A6NNW6
FunCoupENSG00000188316
BioGRIDENO4
STRING (EMBL)ENO4
ZODIACENO4
Ontologies - Pathways
QuickGOA6NNW6
Ontology : AmiGOphosphopyruvate hydratase complex  magnesium ion binding  molecular_function  phosphopyruvate hydratase activity  cellular_component  glycolytic process  biological_process  
Ontology : EGO-EBIphosphopyruvate hydratase complex  magnesium ion binding  molecular_function  phosphopyruvate hydratase activity  cellular_component  glycolytic process  biological_process  
NDEx NetworkENO4
Atlas of Cancer Signalling NetworkENO4
Wikipedia pathwaysENO4
Orthology - Evolution
OrthoDB387712
GeneTree (enSembl)ENSG00000188316
Phylogenetic Trees/Animal Genes : TreeFamENO4
HOVERGENA6NNW6
HOGENOMA6NNW6
Homologs : HomoloGeneENO4
Homology/Alignments : Family Browser (UCSC)ENO4
Gene fusions - Rearrangements
Fusion: Tumor Portal ENO4
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerENO4 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)ENO4
dbVarENO4
ClinVarENO4
1000_GenomesENO4 
Exome Variant ServerENO4
ExAC (Exome Aggregation Consortium)ENSG00000188316
GNOMAD BrowserENSG00000188316
Genetic variants : HAPMAP387712
Genomic Variants (DGV)ENO4 [DGVbeta]
DECIPHERENO4 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisENO4 
Mutations
ICGC Data PortalENO4 
TCGA Data PortalENO4 
Broad Tumor PortalENO4
OASIS PortalENO4 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICENO4  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDENO4
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 ENO4
DgiDB (Drug Gene Interaction Database)ENO4
DoCM (Curated mutations)ENO4 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)ENO4 (select a term)
intoGenENO4
Cancer3DENO4(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM131375   
Orphanet
MedgenENO4
Genetic Testing Registry ENO4
NextProtA6NNW6 [Medical]
TSGene387712
GENETestsENO4
Target ValidationENO4
Huge Navigator ENO4 [HugePedia]
snp3D : Map Gene to Disease387712
BioCentury BCIQENO4
ClinGenENO4
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD387712
Chemical/Pharm GKB GenePA165548527
Clinical trialENO4
Miscellaneous
canSAR (ICR)ENO4 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineENO4
EVEXENO4
GoPubMedENO4
iHOPENO4
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Thu Nov 9 11:45:47 CET 2017

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